VANCE PHILIPS FOLLOWER CATHETER & BOUGIE— 510(k) K792221

Name: FDA 510(k) clearance K792221
Creator: U.S. Food and Drug Administration
Published: 1979-12-06

Substantially Equivalent

Vance Products, Inc.

FDA 510(k) clearance K792221 for VANCE PHILIPS FOLLOWER CATHETER & BOUGIE, Substantially Equivalent on 1979-12-06. Applicant: Vance Products, Inc.. Device class: 2.

Clearance details

Applicant: Vance Products, Inc.
Product code: Code KOE
Device class: Class 2
Regulation: 21 CFR 876.5520
Advisory panel: Gastroenterology, Urology
Date received: 1979-11-05
Decision date: 1979-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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