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..

Clearance details

Applicant: Quinton, Inc.
Product code: Code KGZ
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 ↗

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