ROBICSEK PROBE/RETRACTOR— 510(k) K910682

Substantially Equivalent

Bio-Vascular, Inc.

FDA 510(k) clearance K910682 for ROBICSEK PROBE/RETRACTOR, Substantially Equivalent on 1991-05-08. Applicant: Bio-Vascular, Inc..

Clearance details

Applicant: Bio-Vascular, Inc.
Product code: Code DWP
Advisory panel: Cardiovascular
Date received: 1991-02-19
Decision date: 1991-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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