Medical Device Manufacturer · US , Palo Alto , CA

Intex Research & Development Center - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985
1
Total
1
Cleared
0
Denied

Intex Research & Development Center has 1 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Intex Research & Development Center Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Intex Research & Development Center

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