Medical Device Manufacturer · CA , Markham, Ontario

Quinton Electrophysiology Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1989

Recent clearances: EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391, EP AMP, MODEL #901, EPLAB (ELECTROCARDIOGRAPHIC MONITOR)

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Quinton Electrophysiology Corp. Cardiovascular ✕

3 devices

1-3 of 3

Cleared Dec 29, 1997

EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391

Cardiovascular · 244d

Cleared Apr 30, 1993

EP AMP, MODEL #901

Cardiovascular · 190d

Cleared Sep 08, 1989

EPLAB (ELECTROCARDIOGRAPHIC MONITOR)

Cardiovascular · 107d