Medline Non-Surgical Isolation Gown-

FDA 510(k) K160471 · Medline Industries, Inc.

Substantially Equivalent

510(k) numberK160471

Submission

Device name
Medline Non-Surgical Isolation Gown-
Applicant
Medline Industries, Inc.
Mundelein, IL, US
Received
February 19, 2016
Decision date
January 31, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FYC – Gown, Isolation, Surgical
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

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K223304Disposable Isolation Gowns (S,M,L,XL,XXL,XXXL)FYC · Traditional Xiamen Probtain Medical Technology Co., Ltd.02/08/2023SE
K223411Disposable Isolation Gowns (S,M,L,XL,XXL,XXXL)FYC · Traditional Xiamen Probtain Medical Techology Co., Ltd.01/04/2023SE
K212717Paneffort AAMI Level 3 Isolation GownFYC · Traditional Paneffort, LLC11/30/2022SE
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K214116AAMI4 Isolation GownFYC · Traditional Hubei Xinxin Non-Woven Co., Ltd.10/11/2022SE
K221027Isolation Gown (S, M, L, XL, XXL (Yellow, Blue))FYC · Traditional Allmed Medical (Hubei) Protective Products Co.…08/12/2022SE
K220528Surgical Isolation Cover GownFYC · Traditional Wuhan Dymex Healthcare Co., Ltd.06/10/2022SE

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Questions and answers

When was Medline Non-Surgical Isolation Gown- cleared by the FDA?

Medline Non-Surgical Isolation Gown- (K160471) received a 510(k) decision of Substantially Equivalent on January 31, 2017, 347 days after the submission was received.

What is the product code of K160471?

The FDA product code is FYC – Gown, Isolation, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4040.