MAHURKAR FEMORAL CATHETER— 510(k) K830674

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K830674 for MAHURKAR FEMORAL CATHETER, Substantially Equivalent on 1983-05-18. Applicant: Quinton, Inc.. Device class: 2.

Clearance details

Applicant: Quinton, Inc.
Product code: Code LFK
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1983-03-04
Decision date: 1983-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

Download summary PDF View on FDA.gov ↗

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K891763 — FC-100 FEMORAL CATHETER1989-04-07
K891764 — FC-101 FEMORAL CATHETER GUIDE WIRE1989-04-07

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