Medical Device Manufacturer · US , Portland , OR

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

2 submissions · 2 cleared · Since 1991

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Disco, Inc. Cardiovascular ✕

2 devices

1-2 of 2

Cleared Feb 12, 1993

QUICKLAMP SYSTEM

Cardiovascular · 232d

Cleared Dec 13, 1991

FEMORAL ARTERY PRESSURE PAD/DISK

Cardiovascular · 88d