Ximed/Prosure/Injectx
Ximed/Prosure/Injectx appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 4, 2001.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K002269 | ELECTROSURGICAL PROBES AND DEVICES-GELTX | January 4, 2001 |
| K994151 | PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES | March 1, 2000 |
| K983200 | INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX | December 11, 1998 |
| K983765 | INJECTION NEEDLE PROBE/DEVICE-TUNIS | December 11, 1998 |
| K981256 | ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODE | May 12, 1998 |
| K974484 | ISOLATED ELECTROSURGICAL PROBES AND DEVICES-SALINETRODE | February 10, 1998 |
| K974637 | ELECTRODES/PROBES/DEVICES | January 7, 1998 |
| K962593 | ELECTROSURGICAL PROBES & DEVICES | November 12, 1996 |
| K945995 | BIPOLAR ELECTROSURGICAL PROBES AND INSTRUMENTS | January 31, 1995 |