Life-Tech Intl., Inc.
FDA 510(k) & PMA Approved Devices — 68 products
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Total Devices68
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K001129 | PROLONG, MODELS PL50, PL100, PL150 | CAZ | 2000-07-06 | View |
| 510(k) | K955031 | MAXISTIM | KOI | 1996-12-10 | View |
| 510(k) | K954505 | EZ STIM | KOI | 1996-12-10 | View |
| 510(k) | K954315 | PVC ABDOMINAL/RECTAL PRESSURE CATHETER | FEN | 1995-11-30 | View |
| 510(k) | K954341 | URODYNAMICS TUBING AND INFUSION SETS | FEN | 1995-10-17 | View |
| 510(k) | K953451 | UROPUMP TUBE & DAMPING CHAMGER | FEN | 1995-10-05 | View |
| 510(k) | K953353 | UROVISION JANUS | FEN | 1995-09-08 | View |
| 510(k) | K946108 | EAR-A-GATOR | KHH | 1995-06-13 | View |
| 510(k) | K913601 | MICROPHOR | EGJ | 1994-07-15 | View |
| 510(k) | K940203 | TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS | FEN | 1994-03-30 | View |
| 510(k) | K931179 | UROLAB SPECTRUM | FAP | 1993-11-18 | View |
| 510(k) | K931282 | VOLUME TRANSDUCER | EXQ | 1993-09-17 | View |
| 510(k) | K923634 | MODIFIED F-10 CULTURE MEDIUM | MFD | 1993-09-07 | View |
| 510(k) | K923652 | DULBECCO'S PHOSPHATE BUFFERED SALINE | MFD | 1993-09-07 | View |
| 510(k) | K923612 | MODIFIED F-10 CULTURE MEDIUM W/O HYPOXANTHINE | MFD | 1993-09-07 | View |
| 510(k) | K923651 | DISTILLED WATER | MFD | 1993-09-07 | View |
| 510(k) | K926349 | PROBLOC INSULATED NEEDLES | GXZ | 1993-07-29 | View |
| 510(k) | K923072 | HANDTYMP | ETY | 1993-03-18 | View |
| 510(k) | K923073 | AUTOMATIC TYMPANOMETER | ETY | 1993-02-19 | View |
| 510(k) | K923071 | DANPLEX DIAGNOSTIC AUDIOMETER, CLIN. DIAG. AUDIOMT | ESD | 1992-09-28 | View |
No matching devices.
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