Medical Device Manufacturer · US , N. Attleboro , MA

Medical Device Consultants, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1982

14

Total

14

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medical Device Consultants, Inc. Hematology ✕

2 devices

1-2 of 2

Cleared Apr 04, 1986

HEMOTEC ACT HIGH RANGE ACTIVATED CLOTTING TIME

Hematology · 80d

Cleared Oct 04, 1985

ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES

Hematology · 66d