Medical Device Manufacturer · US , Sunnyvale , CA

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

2 submissions · 1 cleared · Since 2008
2
Total
1
Cleared
0
Denied

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

Historical record: 1 cleared submissions from 2008 to 2012. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Pathwork Diagnostics, Inc.
2 devices
1-2 of 2
Cleared May 17, 2012
TISSUE OF ORIGIN TEST KIT FFPE
K120489 · OIW
Pathology · 90d
Cleared Jul 30, 2008
PATHWORK DIAGNOSTICS TISSUE OF ORIGIN TEST
K080896 · OIW
Pathology · 121d
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