Device Classification Name |
System, X-Ray, Stationary
|
510(k) Number |
K050151 |
Device Name |
MULTIDIAGNOST ELEVA |
Applicant |
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. |
22100 BOTHELL EVERETT HWY |
P.O. BOX 3003 |
BOTHELL,
WA
98021 -8431
|
|
Applicant Contact |
LYNN HARMER |
Correspondent |
REGULATORY TECHNOLOGY SERVICES, LLC |
1000 Westgate Drive, |
Suite 510k |
Saint Paul,
MN
55114
|
|
Correspondent Contact |
MARK JOB |
Regulation Number | 892.1680
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 01/24/2005 |
Decision Date | 02/09/2005 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Radiology
|
510k Review Panel |
Radiology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
Yes
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|