VASCULAR PROBE, VASCULAR PROBE ES— 510(k) K130896

Substantially Equivalent

Synovis Life Technologies, Inc.

FDA 510(k) clearance K130896 for VASCULAR PROBE, VASCULAR PROBE ES, Substantially Equivalent on 2013-04-24. Applicant: Synovis Life Technologies, Inc..

Clearance details

Applicant
Synovis Life Technologies, Inc.
Product code
Code DWP
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
St. Paul, MN, US
Download summary PDFView on FDA.gov ↗

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