Medical Device Manufacturer · JP , Mie-Ken

Konica Medical and Graphic Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Recent clearances: KONICA LASER IMAGER, MODEL DRYPRO MODEL 771

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Konica Medical and Graphic Corporation Radiology ✕

1 devices

1-1 of 1

Cleared Sep 24, 2003

KONICA LASER IMAGER, MODEL DRYPRO MODEL 771

Radiology · 26d