FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RIGHT ARTERIAL CATHETER

K Number: K822910 · Decision Nov 29, 1982
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
64
Applicant Total
164
Review Days
59

Basic Information

Device Name
RIGHT ARTERIAL CATHETER
K Number
K822910
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
QUINTON, INC.
Date Received
October 1, 1982
Decision Date
November 29, 1982
Product Code
LFJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LFJ Catheter, Subclavian

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LFJ), ordered by most recent decision date.

View all

Other Clearances by QUINTON, INC.

K Number Device Name
K032038 PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601
K021906 QUINTON Q-CATH, MODEL 000460
K003576 Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
K001492 QUINTON Q-STRESS, MODEL 000483
K992908 Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)
K990866 QUINTON MEDTRACK CR PLUS TREADMILL
K971397 VIEWCATH 3-D CATHETER PULLBACK
K964784 SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431)
K964978 VITAL STATISTICS SYSTEM (O-CATH ACCESSORY)
K955002 MAHURKAR 8 FR DUAL LEMEN CATHETER
Search all 164 clearances from QUINTON, INC. →