Medical Device Manufacturer · IN , Pune

Periwinkle Technologies Pvt., Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Periwinkle Technologies Pvt., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Pune, IN.

Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Obstetrics & Gynecology.

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

510(k) submissions have been managed by IZiel Healthcare as regulatory consultant.

FDA 510(k) Regulatory Record - Periwinkle Technologies Pvt., Ltd.
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