PERI-PATCH GLUE MOLD— 510(k) K810530

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K810530 for PERI-PATCH GLUE MOLD, Substantially Equivalent on 1981-03-24. Applicant: Quinton, Inc.. Device class: 1.

Clearance details

Applicant: Quinton, Inc.
Product code: Code KGZ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1981-02-26
Decision date: 1981-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.