Wr Medical Electronics Co.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K092809 | HRV ACQUIRE | October 19, 2010 |
| K063560 | HILGER DUAL-STIM NERVE STIMULATOR | January 5, 2007 |
| K000574 | IONTOPHORETIC DRUG DELIVERY ELECTRODE, IONTOPHORETIC ELECTRODE (ACTIVE) | August 9, 2000 |
| K992874 | Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM | November 18, 1999 |
| K910624 | CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 | January 17, 1992 |
| K895838 | BRACKMANN EMG MONITORING SYSTEM | March 27, 1990 |