ADHESIVE REMOVER— 510(k) K821162

Name: FDA 510(k) clearance K821162
Creator: U.S. Food and Drug Administration
Published: 1982-05-14

Substantially Equivalent

The Healthcare Group Laboratories, Inc.

FDA 510(k) clearance K821162 for ADHESIVE REMOVER, Substantially Equivalent on 1982-05-14. Applicant: The Healthcare Group Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: The Healthcare Group Laboratories, Inc.
Product code: Code KOX
Device class: Class 1
Regulation: 21 CFR 878.4730
Advisory panel: General, Plastic Surgery
Date received: 1982-04-26
Decision date: 1982-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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