Medical Device Manufacturer · US , Mahwah , NJ

Seiko Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988
2
Total
2
Cleared
0
Denied

Seiko Corp. has 2 FDA 510(k) cleared medical devices. Based in Mahwah, US.

Historical record: 2 cleared submissions from 1988 to 1990. Primary specialty: Ophthalmic.

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

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