Physio Technology, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K883893 | OMNISOUND(TM) 3000 | IMG | 1988-11-01 | View |
| 510(k) | K874076 | MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR | IPF | 1988-01-04 | View |
| 510(k) | K861039 | OMNIVAC (VACUUM ELECTRODE SYSTEM) | LIH | 1986-09-26 | View |
| 510(k) | K850850 | AUTOMOVE/OMNISTIM IV-ELECTRICAL MUSCLE STIMULATOR | IPF | 1985-07-01 | View |
| 510(k) | K850851 | G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S | ISA | 1985-06-25 | View |
| 510(k) | K850849 | MYOMETER EMG BIOFEEDBACK DEVICE | HCC | 1985-05-31 | View |
| 510(k) | K843351 | OMNISTIM II COMBIN. THERAPY SYS | IMG | 1984-09-18 | View |
| 510(k) | K843372 | OMNISOUND THERAPY UNIT | IMI | 1984-09-18 | View |
| 510(k) | K841874 | MEGA PULSE THERAPY UNIT | IMJ | 1984-05-31 | View |
| 510(k) | K841278 | OMNISTIM III INTERFERENTIAL THERAPY | IPF | 1984-04-24 | View |
No matching devices.
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