SCAREASE & SCAREASE ADHESIVE GEL— 510(k) K984115

Name: FDA 510(k) clearance K984115
Creator: U.S. Food and Drug Administration
Published: 1999-02-12

Substantially Equivalent

Scarease, Inc.

FDA 510(k) clearance K984115 for SCAREASE & SCAREASE ADHESIVE GEL, Substantially Equivalent on 1999-02-12. Applicant: Scarease, Inc.. Device class: 1.

Clearance details

Applicant: Scarease, Inc.
Product code: Code MDA
Device class: Class 1
Regulation: 21 CFR 878.4025
Advisory panel: General, Plastic Surgery
Date received: 1998-11-17
Decision date: 1999-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Poway, CA, US

Download summary PDF View on FDA.gov ↗

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