Medispec, Ltd. - FDA 510(k) Cleared Devices
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
Cleared
Jan 27, 2023
Omnispec ED1000
Physical Medicine
736d
Cleared
Mar 09, 2007
ECONOLITH EM1000
Gastroenterology & Urology
109d
Cleared
May 25, 2004
ECONOLITH E3000, MODEL 3000 (SW-6)
Gastroenterology & Urology
92d
Cleared
Mar 12, 1998
LITHOSPEC(TM) INTRACORPOREAL LITHOTRIPTER
Gastroenterology & Urology
80d