Medical Device Manufacturer · US , New York , NY

Konica Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Konica Corp. Radiology ✕

5 devices

1-5 of 5

Cleared Oct 29, 1999

KONICA LASER IMAGER, DRYPRO MODEL 722

Radiology · 88d

Cleared Aug 17, 1999

KONICA DIRECT DIGITIZER, MODEL DD-341

Radiology · 193d

Cleared Jun 19, 1998

KONICA DIRECT DIGITIZER REGIUS MODEL 330

Radiology · 105d

Cleared May 06, 1992

KONICA LI 10 AND 10A LASER IMAGER

Radiology · 90d

Cleared Mar 06, 1992

KONICA DIRECT DIGITIZER KD-1000

Radiology · 84d