BAND-AID BRAND TRICOT MESH BANDAGES— 510(k) K801823

Name: FDA 510(k) clearance K801823
Creator: U.S. Food and Drug Administration
Published: 1980-08-20

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K801823 for BAND-AID BRAND TRICOT MESH BANDAGES, Substantially Equivalent on 1980-08-20. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code KGY
Device class: Class 1
Regulation: 21 CFR 878.4100
Advisory panel: General, Plastic Surgery
Date received: 1980-07-31
Decision date: 1980-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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K801824 — BAND-AID BRAND FLEXIBLE FABRIC BANDAGE1980-08-20

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Data sourced from openFDA. This site is unofficial and independent of the FDA.