Ximed/Prosure/Injectx - FDA 510(k) Cleared Devices
Recent clearances: PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES, INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX, INJECTION NEEDLE PROBE/DEVICE-TUNIS
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ximed/Prosure/Injectx General & Plastic Surgery ✕
6 devices
Cleared
Jan 04, 2001
ELECTROSURGICAL PROBES AND DEVICES-GELTX
General & Plastic Surgery
162d
Cleared
Mar 01, 2000
PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES
General & Plastic Surgery
83d
Cleared
Dec 11, 1998
INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX
General & Plastic Surgery
88d
Cleared
Feb 10, 1998
ISOLATED ELECTROSURGICAL PROBES AND DEVICES-SALINETRODE
General & Plastic Surgery
76d
Cleared
Nov 12, 1996
ELECTROSURGICAL PROBES & DEVICES
General & Plastic Surgery
133d
Cleared
Jan 31, 1995
BIPOLAR ELECTROSURGICAL PROBES AND INSTRUMENTS
General & Plastic Surgery
117d