Medical Device Manufacturer · US , Mchenry , IL

Quinton, Inc. - FDA 510(k) Cleared Devices

164 submissions · 160 cleared · Since 1976

Recent clearances: PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601, QUINTON Q-CATH, MODEL 000460, Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503

164

Total

160

Cleared

0

Denied

FDA 510(k) Regulatory Record - Quinton, Inc. General & Plastic Surgery ✕

5 devices

1-5 of 5

Cleared Oct 11, 1989

MODIFIED SUTURE USED IN CATHETER INSERTION TRAYS

General & Plastic Surgery · 184d

Cleared Aug 04, 1987

MODIFIED CURLCATH

General & Plastic Surgery · 22d

Cleared Mar 24, 1981

PERI-PATCH GLUE MOLD

General & Plastic Surgery · 26d

Cleared Mar 24, 1981

PERI-PATCH PERITONEAL CATHETER EXTENSION

General & Plastic Surgery · 26d

Cleared Aug 04, 1980

BETA-CAP II ADAPTER

General & Plastic Surgery · 13d