510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K213832Substantially Equivalent

AAMI3 Isolation Gown

Hubei Xinxin Non-woven Co., Ltd, Xiantao, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K213832 is the FDA 510(k) clearance record for AAMI3 Isolation Gown, a class II device, cleared for Hubei Xinxin Non-Woven Co., Ltd. on under FDA product code FYC (Gown, Isolation, Surgical). FDA records list 4 510(k) clearances for Hubei Xinxin Non-Woven Co., Ltd., from to . As of , FDA records show no recalls naming K213832.

Clearance record

Decision date
Received
(158 days to decision)
Product code
FYC Gown, Isolation, Surgical
Regulation
21 CFR 878.4040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Hubei Xinxin Non-Woven Co., Ltd. Taizihu Industrial Park, Pengchang Town, Xiantao, CN
510(k) summary
Statement
Third party review
No

Clearances, product code FYC

Trailing 12 months

FDA records hold no clearances under product code FYC in the trailing twelve months.

FDA records show no clearances under product code FYC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FYC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260