PERCUTANEOUS SURAPUBIC CATHETER— 510(k) K780765

Name: FDA 510(k) clearance K780765
Creator: U.S. Food and Drug Administration
Published: 1978-07-17

Substantially Equivalent

Vance Products, Inc.

FDA 510(k) clearance K780765 for PERCUTANEOUS SURAPUBIC CATHETER, Substantially Equivalent on 1978-07-17. Applicant: Vance Products, Inc.. Device class: 2.

Clearance details

Applicant: Vance Products, Inc.
Product code: Code KOB
Device class: Class 2
Regulation: 21 CFR 876.5090
Advisory panel: Gastroenterology, Urology
Date received: 1978-05-05
Decision date: 1978-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K812785 — VANCE-AMBROSE RESECTOSCOPE FORCEPS1981-11-16
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