Medical Device Manufacturer · US , Stratford , CT

Dianon Systems, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1987

2

Total

1

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Jul 11, 1988

CODE #D2020-FINE NEEDLE ASPIRATION BIOPSY SYSTEM

General & Plastic Surgery · 53d

Cleared Jul 28, 1987

FINE NEEDLE ASPIRATION BIOPSY SYSTEM-PROSTATE

General & Plastic Surgery · 26d