Medical Device Manufacturer · US , Germantown , MD

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

4 submissions · 4 cleared · Since 1998
4
Total
4
Cleared
0
Denied

Medispec, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Germantown, US.

Last cleared in 2023. Active since 1998. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) cleared devices by Medispec, Ltd.

4 devices
1-4 of 4
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