Medical Device Manufacturer · US , Northridge , CA

Xenotope Diagnostics, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003
1
Total
1
Cleared
0
Denied

Xenotope Diagnostics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Northridge, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Microbiology.

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

FDA 510(k) Regulatory Record - Xenotope Diagnostics, Inc.

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