Medical Device Manufacturer · US , Walker , MI

Cartaya Assoc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1980
1
Total
1
Cleared
0
Denied

Cartaya Assoc. has 1 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 1 cleared submissions from 1980 to 1980. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Cartaya Assoc.
1 devices
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