Medical Device Manufacturer · US , Cherry Hill , NJ

D.Y. Instrument, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Recent clearances: AIS100 AUTOMATIC INTRAMUSCULAR STIMULATOR

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - D.Y. Instrument, Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared Aug 26, 2004

AIS100 AUTOMATIC INTRAMUSCULAR STIMULATOR

General Hospital · 175d