Ep Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 15 products
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Total Devices15
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K043257 | REAL-TIME POSITION MANAGEMENT (RPM) SYSTEM | DRF | 2005-02-03 | View |
| 510(k) | K013349 | ASTRONOMER PLUS SYSTEM | DQK | 2002-04-09 | View |
| 510(k) | K003452 | POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006D | DRF | 2000-12-07 | View |
| 510(k) | K940167 | DIAGNOSTIC I CATHETER | DRF | 1994-08-02 | View |
| 510(k) | K940168 | DIAGNOSTIC II CATHETER | DRF | 1994-07-27 | View |
| 510(k) | K924108 | TRACFINDER II | DRF | 1993-12-16 | View |
| 510(k) | K924109 | STEEROCATH II | DRF | 1993-12-16 | View |
| 510(k) | K913375 | TORQUE TUBE STEEROCATH(TM) | DRF | 1991-10-25 | View |
| 510(k) | K903880 | FRANZ(TM) STEERABLE COMBINATION CATHETER | DRF | 1990-10-12 | View |
| 510(k) | K900765 | STEEROCATH(TM) | DRF | 1990-05-07 | View |
| 510(k) | K900452 | QUATTRO CATHETER | DRF | 1990-03-14 | View |
| 510(k) | K900553 | CONSTANT CURRENT STIMULATOR MODEL 022101 | JOQ | 1990-03-13 | View |
| 510(k) | K892207 | FRANZ(TM) MOVEABLE STYLET MAP CATHETER, MODIFIED | DRF | 1989-06-12 | View |
| 510(k) | K885252 | MAP DC-COUPLED ISOLATED PREAMPLIFIER MODEL #1001 | DRQ | 1989-01-13 | View |
| 510(k) | K881853 | FRANZ CATHETER | DRF | 1988-07-18 | View |
No matching devices.
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