Myo/Kinetic Systems, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K945937 | TE-800 PELVIC FLOOR EXERCISER | HIR | 1995-07-14 | View |
| 510(k) | K945292 | TS-700P CONTROL XP ELECTRICAL STIMULATOR | KPI | 1995-04-12 | View |
| 510(k) | K944972 | URO-GRAM CYSTOMRTROGRAM WITH UROFLOWMETRY | EXY | 1995-03-08 | View |
| 510(k) | K936041 | UROGRAM CYSTOMETROGRAM | FEN | 1994-04-18 | View |
| 510(k) | K932611 | NEUROMUSCULAR STIMULATOR | GZJ | 1994-01-31 | View |
| 510(k) | K932764 | THERAPEUTIC STIMULATOR 300(TS-300) & 300P(TS-300P) | IPF | 1993-10-01 | View |
| 510(k) | K932399 | THERAPEUTIC STIM 200 (TS-200)/200P (TS-200P) | IPF | 1993-08-11 | View |
| 510(k) | K914904 | THERAPEUTIC STIMULATOR 2100 (TS-2100) | IPF | 1992-04-28 | View |
No matching devices.
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