Medical Device Manufacturer · IL , Kfar Saba

Annabella , Ltd. - FDA 510(k) Cleared Devices

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

Annabella , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Kfar Saba, IL.

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

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

510(k) submissions have been managed by Dalia Dickman Consulting as regulatory consultant.

FDA 510(k) Regulatory Record - Annabella , Ltd.
1 devices
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