510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K221038Substantially Equivalent

Disposable Medical Masks

Hantech Medical Device Co., Ltd., Ningbo, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K221038 is the FDA 510(k) clearance record for Disposable Medical Masks, a class II device, cleared for Hantech Medical Device Co., Ltd. on under FDA product code FXX (Mask, Surgical). FDA records list 5 510(k) clearances for Hantech Medical Device Co., Ltd., from to . As of , FDA records show no recalls naming K221038.

Clearance record

Decision date
Received
(147 days to decision)
Product code
FXX Mask, Surgical
Regulation
21 CFR 878.4040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Hantech Medical Device Co., Ltd. No 288, Sanheng Rd. Changhe Industridal Park, Cixi, Ningbo, CN
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code FXX

Trailing 12 months
8 clearances under product code FXX in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FXX, trailing twelve months
MonthClearances
November 20251
December 20252
January 20262
February 20261
March 20262
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260