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.. Device class: 2.

Clearance details

Applicant
Synovis Life Technologies, Inc.
Product code
Code DWP
Device class
Class 2
Regulation
21 CFR 870.4475
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
St. Paul, MN, US
Download summary PDFView on FDA.gov ↗

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Recalls naming K130896

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K130896.

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