Medical Device Manufacturer · CH , Solothurn

Medical Instruments Corporation, AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Recent clearances: MODIFICATION TO: PRONTO DRY

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medical Instruments Corporation, AG Microbiology ✕

1 devices

1-1 of 1

Cleared Sep 29, 2000

MODIFICATION TO: PRONTO DRY

Microbiology · 51d