Cleared Traditional

K223467 - Disposable Isolation Gown (FDA 510(k) Clearance)

Feb 2023
Decision
85d
Days
Class 2
Risk

K223467 is an FDA 510(k) clearance for the Disposable Isolation Gown. This device is classified as a Gown, Isolation, Surgical (Class II - Special Controls, product code FYC).

Submitted by Nanning Tecbod Biological Technology Co., Ltd. (Naning, CN). The FDA issued a Cleared decision on February 10, 2023, 85 days after receiving the submission on November 17, 2022.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 878.4040.

Submission Details

510(k) Number K223467 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 17, 2022
Decision Date February 10, 2023
Days to Decision 85 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code FYC - Gown, Isolation, Surgical
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4040