Medical Device Manufacturer · US , Wellesley , MA

Intera Oncology, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

Intera Oncology, Inc. has 2 FDA 510(k) cleared medical devices. Based in Wellesley, US.

Last cleared in 2022. Active since 2021. Primary specialty: General Hospital.

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

510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Intera Oncology, Inc.
2 devices
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