HERMITEX SPONGE— 510(k) K891324

Name: FDA 510(k) clearance K891324
Creator: U.S. Food and Drug Administration
Published: 1989-04-27

Substantially Equivalent

Hermitage Hospital Products, Inc.

FDA 510(k) clearance K891324 for HERMITEX SPONGE, Substantially Equivalent on 1989-04-27. Applicant: Hermitage Hospital Products, Inc.. Device class: 1.

Clearance details

Applicant: Hermitage Hospital Products, Inc.
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1989-03-13
Decision date: 1989-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Niantic, CT, US

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