510(k) K213832

Device
AAMI3 Isolation Gown
Applicant
Hubei Xinxin Non-Woven Co., Ltd.
510(k) number
K213832
Product code
FYC
Decision
Substantially Equivalent (SESE)
Decision date
2022-05-16
Date received
2021-12-09
Regulation
878.4040
Classification name
Gown, Isolation, Surgical
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Nicole Jin
Address
Taizihu Industrial Park, Pengchang Town Xiantao CN 433018 433018

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

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