HASKON MEDICAL GRADE SHEETING— 510(k) K934829

Name: FDA 510(k) clearance K934829
Creator: U.S. Food and Drug Administration
Published: 1994-02-03

Substantially Equivalent

Haskon Intl., Inc.

FDA 510(k) clearance K934829 for HASKON MEDICAL GRADE SHEETING, Substantially Equivalent on 1994-02-03. Applicant: Haskon Intl., Inc.. Device class: 1.

Clearance details

Applicant: Haskon Intl., Inc.
Product code: Code MDA
Device class: Class 1
Regulation: 21 CFR 878.4025
Advisory panel: General, Plastic Surgery
Date received: 1993-10-08
Decision date: 1994-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taunton, MA, US

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