Medical Device Manufacturer · US , San Fransisco , CA

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

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Tampro, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Fransisco, US.

Last cleared in 2023. Active since 2023. Primary specialty: Obstetrics & Gynecology.

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

510(k) submissions have been managed by Regulatory and Technical Associates as regulatory consultant.

FDA 510(k) Regulatory Record - Tampro, Inc.
1 devices
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