Medical Device Manufacturer · US , Poway , CA

Sontec, Inc. - FDA 510(k) Cleared Devices

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

Sontec, Inc. has 0 FDA 510(k) cleared medical devices. Based in Poway, US.

Historical record: 0 cleared submissions from 1985 to 1985. Primary specialty: Physical Medicine.

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

FDA 510(k) Regulatory Record - Sontec, Inc.

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All1 Physical Medicine 1