Medical Device Manufacturer · US , Mchenry , IL

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

164 submissions · 160 cleared · Since 1976

164

Total

160

Cleared

0

Denied

69 devices

51-69 of 69

Cleared Oct 20, 1983

ULTRA LIGHT RAAF CATHETER

Cardiovascular · 65d

Cleared Jul 18, 1983

STAINLESS STEEL GUIDE WIRE

Cardiovascular · 41d

Cleared Jun 15, 1983

QUIK-SILVER RESTING ECG ELECTRODE

Cardiovascular · 105d

Cleared Sep 14, 1982

SINGLE CHANNEL NONFADE OSCILLOSCOPE

Cardiovascular · 25d

Cleared Aug 25, 1982

QUINTON Q, SCAN MODELS 900 & 901

Cardiovascular · 71d

Cleared Jul 02, 1982

QUIK - PREP2 ELECTRODE

Cardiovascular · 17d

Cleared Apr 29, 1982

QUINTON Q2000 ETT MONITORING SYSTEM

Cardiovascular · 71d

Cleared Jul 28, 1981

SINGLE CHANNEL NON-FADE OSCILLOSCOPE

Cardiovascular · 27d

Cleared Mar 17, 1981

QUINTON LTE ELECTRODE

Cardiovascular · 14d

Cleared Oct 23, 1980

MODEL 633A THREE CHANNEL STRESS TEST

Cardiovascular · 43d

Cleared Dec 19, 1979

WHITE SEALING CAP

Cardiovascular · 85d

Cleared Aug 03, 1979

QUINTON MODEL 630 AND 636 ECG DATA CART

Cardiovascular · 24d

Cleared Apr 26, 1979

QUINTON MODEL 530X ECG DATA CART

Cardiovascular · 10d

Cleared Feb 23, 1979

QUINTON STATUS 1000

Cardiovascular · 72d

Cleared Feb 01, 1979

ELECTRODE SYSTEM, QUIK-PREP

Cardiovascular · 50d

Cleared Mar 28, 1978

ECG MONITORING SYSTEM,

Cardiovascular · 15d

Cleared Feb 21, 1978

STRESS TEST SYSTEM

Cardiovascular · 20d

Cleared Nov 22, 1977

HEARTRATE METER MODEL 650, P/N 000119

Cardiovascular · 15d

Cleared Nov 12, 1976

THREE-CHANNEL STRESS TEST SYSTEM (M633)

Cardiovascular · 28d