Medical Device Manufacturer · JP , Chiba-Ken

Seiko Instruments USA, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997
2
Total
2
Cleared
0
Denied

Seiko Instruments USA, Inc. has 2 FDA 510(k) cleared medical devices. Based in Chiba-Ken, JP.

Historical record: 2 cleared submissions from 1997 to 1999. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Seiko Instruments USA, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Seiko Instruments USA, Inc.
2 devices
1-2 of 2
Cleared Jun 30, 1999
COLORPOINT 1720 MEDICAL IMAGERS AND VIDEO CAPTURE BOX CX-1000 SERIES
K991282 · LMC
Radiology · 77d
Cleared Oct 01, 1997
COLORPOINT OR PROFESSIONAL COLORPOINT
K971760 · LMC
Radiology · 142d
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