Medical Device Manufacturer · MX , Mexico City

Alandra Medical Sapi DE CV - FDA 510(k) Cleared Devices

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

Alandra Medical Sapi DE CV has 1 FDA 510(k) cleared medical devices. Based in Mexico City, MX.

Latest FDA clearance: Sep 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Alandra Medical Sapi DE CV Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

FDA 510(k) Regulatory Record - Alandra Medical Sapi DE CV
1 devices
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