REMOVE ADHESIVE REMOVER— 510(k) K893603

Name: FDA 510(k) clearance K893603
Creator: U.S. Food and Drug Administration
Published: 1989-07-14

Substantially Equivalent

Smith & Nephew United, Inc.

FDA 510(k) clearance K893603 for REMOVE ADHESIVE REMOVER, Substantially Equivalent on 1989-07-14. Applicant: Smith & Nephew United, Inc.. Device class: 1.

Clearance details

Applicant: Smith & Nephew United, Inc.
Product code: Code KOX
Device class: Class 1
Regulation: 21 CFR 878.4730
Advisory panel: General, Plastic Surgery
Date received: 1989-05-16
Decision date: 1989-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

Download summary PDF View on FDA.gov ↗

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