Geiger Medical Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K002341 | THERMAL CAUTERY UNIT, MODEL 150 | October 23, 2000 |
| K001029 | GEIGER NEEDLE ADAPTER, MODEL 406 | May 23, 2000 |
| K994075 | GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435 | December 27, 1999 |
| K992149 | GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405 | August 19, 1999 |
| K983852 | BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429 | January 28, 1999 |