Medical Device Manufacturer · ES , Spain

Palex Intl. SA - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1990

Total

Cleared

Denied

Palex Intl. SA has 5 FDA 510(k) cleared medical devices. Based in Spain, ES.

Historical record: 5 cleared submissions from 1990 to 1991. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Palex Intl. SA Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Palex Intl. SA

5 devices

1-5 of 5