FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Nordiwell Surprotect Face Mask

K Number: K210445 · Decision Jun 29, 2021
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
606
Applicant Total
3
Review Days
133

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Nordiwell Surprotect Face Mask
K Number
K210445
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Changzhou Combat Protective Equipment Co., Ltd.
Date Received
February 16, 2021
Decision Date
June 29, 2021
Product Code
FXX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FXX Mask, Surgical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FXX), ordered by most recent decision date.

View all

Other Clearances by Changzhou Combat Protective Equipment Co., Ltd.

K Number Device Name
K210181 Nordiwell Surgical Face Mask
K202615 Nordiwell Medical Face Mask