BANDAGE COMPRESS 2, 3, 4— 510(k) K770410

Name: FDA 510(k) clearance K770410
Creator: U.S. Food and Drug Administration
Published: 1977-06-09

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K770410 for BANDAGE COMPRESS 2, 3, 4, Substantially Equivalent on 1977-06-09. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1977-03-04
Decision date: 1977-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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