K-BAND AND K-CREPE— 510(k) K926072

Substantially Equivalent

Parema , Ltd.

FDA 510(k) clearance K926072 for K-BAND AND K-CREPE, Substantially Equivalent on 1993-03-19. Applicant: Parema , Ltd.. Device class: 1.

Clearance details

Applicant: Parema , Ltd.
Product code: Code NAB
Device class: Class 1
Regulation: 21 CFR 878.4014
Advisory panel: General, Plastic Surgery
Date received: 1992-12-01
Decision date: 1993-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shepshed, Loughborough, Leics., GB

Download summary PDF View on FDA.gov ↗

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