Ximed/Prosure/Injectx
Ximed/Prosure/Injectx holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2001.
Top product codes for Ximed/Prosure/Injectx
Recent clearances by Ximed/Prosure/Injectx
- K002269 — ELECTROSURGICAL PROBES AND DEVICES-GELTX
- K994151 — PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES
- K983200 — INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX
- K983765 — INJECTION NEEDLE PROBE/DEVICE-TUNIS
- K981256 — ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODE
- K974484 — ISOLATED ELECTROSURGICAL PROBES AND DEVICES-SALINETRODE
- K974637 — ELECTRODES/PROBES/DEVICES
- K962593 — ELECTROSURGICAL PROBES & DEVICES
- K945995 — BIPOLAR ELECTROSURGICAL PROBES AND INSTRUMENTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.