Myo/Kinetic Systems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K945937 | TE-800 PELVIC FLOOR EXERCISER | July 14, 1995 |
| K945292 | TS-700P CONTROL XP ELECTRICAL STIMULATOR | April 12, 1995 |
| K944972 | URO-GRAM CYSTOMRTROGRAM WITH UROFLOWMETRY | March 8, 1995 |
| K936041 | UROGRAM CYSTOMETROGRAM | April 18, 1994 |
| K932611 | NEUROMUSCULAR STIMULATOR | January 31, 1994 |
| K932764 | THERAPEUTIC STIMULATOR 300(TS-300) & 300P(TS-300P) | October 1, 1993 |
| K932399 | THERAPEUTIC STIM 200 (TS-200)/200P (TS-200P) | August 11, 1993 |
| K914904 | THERAPEUTIC STIMULATOR 2100 (TS-2100) | April 28, 1992 |