VANCE MALLEABLE TIP FILIFORM— 510(k) K792219

Name: FDA 510(k) clearance K792219
Creator: U.S. Food and Drug Administration
Published: 1979-12-06

Substantially Equivalent

Vance Products, Inc.

FDA 510(k) clearance K792219 for VANCE MALLEABLE TIP FILIFORM, 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 ↗

Recent devices under product code KOE

view all

K191061 — Optilume Basic Urological Balloon Dilation Catheter2020-01-02
K032840 — ATRION MEDICAL QL INFLATION DEVICE2004-03-03
K972964 — ATRION MEDICAL BALLOON CATHETER INFLATION DEVICE1997-10-10
K962611 — BARD EAGLE INFLATION DEVICE1996-10-21
K961904 — AQ HYDROPHILIC DILATORS1996-10-18

More clearances from Vance Products, Inc.

view all

K812995 — VANCE-JACOBELLIS MICROHEMATURIA CATHETER1982-03-01
K820313 — VPI-FAIR URETHRAL STENT1982-03-01
K813278 — VPI URETERAL DILATATION BALLON CATHETER1981-12-18
K812785 — VANCE-AMBROSE RESECTOSCOPE FORCEPS1981-11-16
K812057 — VANCE CYSTOSCOPIC1981-07-31

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