510(k) K210181

Nordiwell Surgical Face Mask by Changzhou Combat Protective Equipment Co., Ltd. — Product Code FXX

K210181 is an FDA 510(k) premarket notification submitted by Changzhou Combat Protective Equipment Co., Ltd. for the device "Nordiwell Surgical Face Mask". The FDA issued a decision of Substantially Equivalent on Mar 9, 2021. The device falls under product code FXX (Mask, Surgical), a Class II device regulated under 21 CFR 878.4040. Changzhou Combat Protective Equipment Co., Ltd. has 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Mar 9, 2021
Date Received
Jan 22, 2021
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mask, Surgical
Device Class
Class II
Regulation Number
878.4040
Review Panel
HO
Submission Type
510(k)