STERILE SUTURE REMOVAL KIT— 510(k) K821502

Substantially Equivalent

Pro-Pak

FDA 510(k) clearance K821502 for STERILE SUTURE REMOVAL KIT, Substantially Equivalent on 1982-07-09. Applicant: Pro-Pak.

Clearance details

Applicant: Pro-Pak
Product code: Code KDD
Advisory panel: General, Plastic Surgery
Date received: 1982-05-19
Decision date: 1982-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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