EMC China Lab

FCC Certification Fees for Handheld Fans

Views :
Update time : 2025-04-24

fcc certification is mainly divided into two modes: fcc sdoc (Supplier's Declaration of Conformity) and fcc id (Certification). The applicable situations for handheld fans are as follows:

 

FCC sdoc

If your handheld fan does not have wireless communication features and is a standard electronic product, it needs to undergo fcc sdoc certification. This certification follows the fcc part 15 B standard, primarily testing electromagnetic interference to ensure the product does not cause harmful interference to nearby radio devices.

For example, a basic handheld fan without features like remote control or Bluetooth would be suitable for this certification.

 

FCC Certification Fees for Handheld Fans(图1)


FCC ID

When a handheld fan has wireless features, such as Bluetooth, Wi-Fi control, or infrared remote control, it must undergo fcc part 15 c certification and apply for an FCC ID.

A handheld fan with Bluetooth functionality, for instance, emits wireless signals during use and requires stricter testing and certification to ensure its wireless transmission does not interfere with other licensed radio services.


fcc certification Cycle and Fees

Certification Cycle

- FCC SDoC certification: Generally takes around 5 to 7 business days.

- fcc id certification: Due to the more complex testing and review process, the cycle typically lasts 2 to 3 weeks.

If the product fails the testing and requires modifications, the certification cycle will be extended accordingly.

 

Certification Fees

- The fees vary depending on the product type, features, testing items, and other factors:

- FCC SDoC certification: Costs are generally around $780.

- FCC ID certification: For products with wireless functionality, the fees could range from $1400 to $2000.


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
Biological Evaluation of Medical Devices ISO 10993 Biological Evaluation of Medical Devices ISO 10993
04 .16.2026
JJR LAB performs ISO 10993 biological evaluations to ensure medical devices are safe for human use, ...
In Vitro Cytotoxicity Test for Biomedical Devices In Vitro Cytotoxicity Test for Biomedical Devices
04 .16.2026
JJR LAB conducts ISO 10993-5 in vitro cytotoxicity tests to ensure medical device safety, assessing ...
EU Responsible Person on Amazon EU Responsible Person on Amazon
04 .16.2026
EU Responsible Person is EU rep for non-EEA manufacturers ensuring compliance and regulatory require...
GPSR EU Responsible Person Service GPSR EU Responsible Person Service
04 .16.2026
EU Responsible Person compliance is essential for selling in Europe, covering requirements, risks, a...
UK Responsible Person for Medical Devices UK Responsible Person for Medical Devices
04 .16.2026
UK rules clarify UK Responsible Person info: required for UKCA, not CE, but always MHRA-registered. ...
UK Cosmetics Responsible Person Service UK Cosmetics Responsible Person Service
04 .16.2026
JJR LAB’s UK Cosmetics Responsible Person Service ensures imported products meet UK labeling rules, ...
FDA Registration US Agent FDA Registration US Agent
04 .15.2026
FDA registration requires foreign mfrs to appoint a US Agent to liaise with FDA, handle inspections,...
ASTM F963 Toy Safety Standard ASTM F963 Toy Safety Standard
04 .15.2026
ASTM F963 defines mandatory toy safety rules covering mechanical chemical electrical flammability an...

Leave Your Message