Ep Technologies, Inc.
Ep Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2005.
Top product codes for Ep Technologies, Inc.
Recent clearances by Ep Technologies, Inc.
- K043257 — REAL-TIME POSITION MANAGEMENT (RPM) SYSTEM
- K013349 — ASTRONOMER PLUS SYSTEM
- K003452 — POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006D
- K940167 — DIAGNOSTIC I CATHETER
- K940168 — DIAGNOSTIC II CATHETER
- K924108 — TRACFINDER II
- K924109 — STEEROCATH II
- K913375 — TORQUE TUBE STEEROCATH(TM)
- K903880 — FRANZ(TM) STEERABLE COMBINATION CATHETER
- K900765 — STEEROCATH(TM)
- K900452 — QUATTRO CATHETER
- K900553 — CONSTANT CURRENT STIMULATOR MODEL 022101
- K892207 — FRANZ(TM) MOVEABLE STYLET MAP CATHETER, MODIFIED
- K885252 — MAP DC-COUPLED ISOLATED PREAMPLIFIER MODEL #1001
- K881853 — FRANZ CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.