NU-GAUZE SPONGE— 510(k) K821150

Name: FDA 510(k) clearance K821150
Creator: U.S. Food and Drug Administration
Published: 1982-08-27

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K821150 for NU-GAUZE SPONGE, Substantially Equivalent on 1982-08-27. Applicant: Johnson & Johnson Professionals, Inc.. Device class: Unclassified.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1982-04-23
Decision date: 1982-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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