PEDIATRIC SIZED HEMOCATH CATHETER— 510(k) K844692

Name: FDA 510(k) clearance K844692
Creator: U.S. Food and Drug Administration
Published: 1985-01-18

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K844692 for PEDIATRIC SIZED HEMOCATH CATHETER, Substantially Equivalent on 1985-01-18. Applicant: Quinton, Inc.. Device class: 2.

Clearance details

Applicant: Quinton, Inc.
Product code: Code FIQ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1984-12-03
Decision date: 1985-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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