Medical Device Manufacturer · US , Rochester , NY

Mdt Biologic Co. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1991

8

Total

8

Cleared

0

Denied

Mdt Biologic Co. has 8 FDA 510(k) cleared medical devices. Based in Rochester, US.

Historical record: 8 cleared submissions from 1991 to 1996. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Mdt Biologic Co. Filter by specialty or product code using the sidebar.

Mdt Biologic Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mdt Biologic Co.

8 devices

1-8 of 8

Cleared Aug 15, 1996

ACCESS (POWERCLAVE)

General Hospital · 304d

Cleared Jan 17, 1996

MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE

General & Plastic Surgery · 79d

Cleared Aug 02, 1995

HARVEY CHEMICLAVE EC5000, EC5500, EC6000 STERILIZERS

General Hospital · 370d

Cleared Aug 09, 1993

CASTLE WASHER/DISINFECTOR, MODEL 7550

General & Plastic Surgery · 882d

Cleared Mar 27, 1992

MDT/CASTLE MODELS S-8 TABLE TOP STEAM STERILIZER

General Hospital · 399d

Cleared Oct 28, 1991

STEAM VACUUM PULSE STERILIZER SYSTEM (SVPSS)

General Hospital · 248d

Cleared Sep 06, 1991

MDT/CASTLE 10/90 LOAD STATION

General Hospital · 204d

Cleared Jun 11, 1991

AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT

General & Plastic Surgery · 97d