510(k) K213832

AAMI3 Isolation Gown by Hubei Xinxin Non-Woven Co., Ltd. — Product Code FYC

K213832 is an FDA 510(k) premarket notification submitted by Hubei Xinxin Non-Woven Co., Ltd. for the device "AAMI3 Isolation Gown". The FDA issued a decision of Substantially Equivalent on May 16, 2022. The device falls under product code FYC (Gown, Isolation, Surgical), a Class II device regulated under 21 CFR 878.4040. Hubei Xinxin Non-Woven Co., Ltd. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 16, 2022
Date Received
December 9, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gown, Isolation, Surgical
Device Class
Class II
Regulation Number
878.4040
Review Panel
HO
Submission Type