PERM-CATH CATHETER KIT— 510(k) K871942

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K871942 for PERM-CATH CATHETER KIT, Substantially Equivalent on 1987-06-17. 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: 1987-05-19
Decision date: 1987-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LFJ

K920780 — MEDSURG INSERTION TRAY1994-08-19
K925819 — AKCESS0CATH KIT1994-08-02
K925818 — AKCESS-CATH1994-04-05
K913468 — ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET/TRAY1994-03-24
K920634 — SPLITTABLE SHEATH INTRODUCER SET1994-01-14

More clearances from Quinton, Inc.

K032038 — PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 926012003-09-05
K021906 — QUINTON Q-CATH, MODEL 0004602002-09-04
K003576 — Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 0005032001-01-25
K001492 — QUINTON Q-STRESS, MODEL 0004832000-08-09
K992908 — Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)2000-03-06

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