Medical Device Manufacturer · GB , United Kingdom

Simport Plastics, Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993
1
Total
1
Cleared
0
Denied

Simport Plastics, Ltd. has 1 FDA 510(k) cleared medical devices. Based in United Kingdom, GB.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Simport Plastics, Ltd.

1 devices
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