EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM


Device Classification Name

catheter, conduction, anesthetic

510(k) Number K023233
Device Name EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM
Original Applicant
EBI, L.P.
399 jefferson road
parsippany, 
NJ 
07054

Original Contact jon caparotta
Regulation Number 868.5120
Classification Product Code
BSO  
Date Received 09/27/2002
Decision Date 12/13/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Anesthesiology

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls