SIREGRAPH CF


Device Classification Name

system, x-ray, fluoroscopic, image-intensified

510(k) Number K960266
Device Name SIREGRAPH CF
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
186 wood avenue south
iselin, 
NJ 
08830

Applicant Contact kathy rutherford
Correspondent
SIEMENS MEDICAL SOLUTIONS USA, INC.
186 wood avenue south
iselin, 
NJ 
08830

Correspodent Contact kathy rutherford
Regulation Number 892.1650
Classification Product Code
JAA  
Date Received 01/18/1996
Decision Date 03/11/1996
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls