510(k) K202139

Medical surgical mask by Guangdong Kingfa Sci. & Tech.Co., Ltd. — Product Code FXX

K202139 is an FDA 510(k) premarket notification submitted by Guangdong Kingfa Sci. & Tech.Co., Ltd. for the device "Medical surgical mask". The FDA issued a decision of Substantially Equivalent on November 20, 2020. The device falls under product code FXX (Mask, Surgical), a Class II device regulated under 21 CFR 878.4040. Guangdong Kingfa Sci. & Tech.Co., Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 20, 2020
Date Received
July 31, 2020
Clearance Type
Traditional
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