Ep Technologies, Inc.

15FDA 510(k) medical device clearances.

Top product codes for Ep Technologies, Inc.

Recent clearances by Ep Technologies, Inc.

K043257 — REAL-TIME POSITION MANAGEMENT (RPM) SYSTEMCode DRF·2005-02-03
K013349 — ASTRONOMER PLUS SYSTEMCode DQK·2002-04-09
K003452 — POLARIS X CATHETERS, MODEL 7000D,7001D,7003D,7004D,7005D,7006DCode DRF·2000-12-07
K940167 — DIAGNOSTIC I CATHETERCode DRF·1994-08-02
K940168 — DIAGNOSTIC II CATHETERCode DRF·1994-07-27
K924108 — TRACFINDER IICode DRF·1993-12-16
K924109 — STEEROCATH IICode DRF·1993-12-16
K913375 — TORQUE TUBE STEEROCATH(TM)Code DRF·1991-10-25
K903880 — FRANZ(TM) STEERABLE COMBINATION CATHETERCode DRF·1990-10-12
K900765 — STEEROCATH(TM)Code DRF·1990-05-07
K900452 — QUATTRO CATHETERCode DRF·1990-03-14
K900553 — CONSTANT CURRENT STIMULATOR MODEL 022101Code JOQ·1990-03-13
K892207 — FRANZ(TM) MOVEABLE STYLET MAP CATHETER, MODIFIEDCode DRF·1989-06-12
K885252 — MAP DC-COUPLED ISOLATED PREAMPLIFIER MODEL #1001Code DRQ·1989-01-13
K881853 — FRANZ CATHETERCode DRF·1988-07-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.