PERMCATH INSERTION TRAY— 510(k) K874633

Unknown

Quinton, Inc.

FDA 510(k) clearance K874633 for PERMCATH INSERTION TRAY, Unknown on 1988-02-17. Applicant: Quinton, Inc.. Device class: 2.

Clearance details

Applicant: Quinton, Inc.
Product code: Code LFJ
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1987-11-09
Decision date: 1988-02-17
Decision: Unknown
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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K920634 — SPLITTABLE SHEATH INTRODUCER SET1994-01-14

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