SINGLE LUMEN ACUTE CATHETER— 510(k) K870328

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K870328 for SINGLE LUMEN ACUTE CATHETER, Substantially Equivalent on 1987-05-11. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code LFJ
Advisory panel: Gastroenterology, Urology
Date received: 1987-01-28
Decision date: 1987-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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