RUSCH GUIDED CHOLANGIOGRAPHY CATHETER


Device Classification Name

catheter, biliary, diagnostic

510(k) Number K023666
Device Name RUSCH GUIDED CHOLANGIOGRAPHY CATHETER
Original Applicant
RUSCH INTL.
50 plantation dr.
jaffery, 
NH 
03452

Original Contact rick lykins
Regulation Number 876.5010
Classification Product Code
FGE  
Date Received 10/31/2002
Decision Date 06/17/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Gastroenterology/Urology

510k Review Panel

Gastroenterology/Urology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No