C-LOOPS— 510(k) K830800

Substantially Equivalent

Concept, Inc.

FDA 510(k) clearance K830800 for C-LOOPS, Substantially Equivalent on 1983-10-04. Applicant: Concept, Inc.. Device class: 1.

Clearance details

Applicant: Concept, Inc.
Product code: Code KDC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1983-03-14
Decision date: 1983-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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.