Medical Device Manufacturer · US , Bailey , CO

Konica Minolta Sensing, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2001

Recent clearances: KONICA MINOLTA PULSOX-300, 300I, MINOLTA PULSOX-2, MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Konica Minolta Sensing, Inc. Anesthesiology ✕

3 devices

1-3 of 3

Cleared May 11, 2006

KONICA MINOLTA PULSOX-300, 300I

Anesthesiology · 154d

Cleared Feb 12, 2003

MINOLTA PULSOX-2

Anesthesiology · 281d

Cleared Aug 02, 2001

MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI

Anesthesiology · 171d