MAGNETOM VERIO


Device Classification Name

system, nuclear magnetic resonance imaging

510(k) Number K072237
Device Name MAGNETOM VERIO
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
51 valley stream pkwy.
malvern, 
PA 
19355 -1406

Applicant Contact judith campbell
Correspondent
SIEMENS MEDICAL SOLUTIONS USA, INC.
51 valley stream pkwy.
malvern, 
PA 
19355 -1406

Correspodent Contact judith campbell
Regulation Number 892.1000
Classification Product Code
LNH  
Date Received 08/13/2007
Decision Date 10/10/2007
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