SCANLAN (TM) VEIN/GRAFT HOLDER— 510(k) K864919

Substantially Equivalent

Scanlan Intl., Inc.

FDA 510(k) clearance K864919 for SCANLAN (TM) VEIN/GRAFT HOLDER, Substantially Equivalent on 1987-01-12. Applicant: Scanlan Intl., Inc..

Clearance details

Applicant: Scanlan Intl., Inc.
Product code: Code KPK
Advisory panel: General, Plastic Surgery
Date received: 1986-12-16
Decision date: 1987-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saint Paul, MN, US

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