VESITEC SUTURE PASSER— 510(k) K931181

Substantially Equivalent

Vesitec Medical, Inc.

FDA 510(k) clearance K931181 for VESITEC SUTURE PASSER, Substantially Equivalent on 1993-05-12. Applicant: Vesitec Medical, Inc.. Device class: 1.

Clearance details

Applicant: Vesitec Medical, Inc.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1993-03-09
Decision date: 1993-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Hills, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Vesitec Medical, Inc.

K932925 — BONE ANCHOR FOR SOFT TISSUE ATTACHMENT1994-04-26
K931182 — VESITEC DRILL GUIDE1993-06-09

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