Device Classification Name |
camera, x-ray, fluorographic, cine or spot
|
510(k) Number |
K920793 |
Device Name |
PHILIPS DSI SYSTEM RELEASE 3.2 |
Applicant |
PHILIPS MEDICAL SYSTEMS, INC. |
VEENPLUIS 4-6 |
P.O. BOX 10000 |
5680 DA BEST,
NL
|
|
Applicant Contact |
WILLIAM G MCMAHON |
Correspondent |
PHILIPS MEDICAL SYSTEMS, INC. |
VEENPLUIS 4-6 |
P.O. BOX 10000 |
5680 DA BEST,
NL
|
|
Correspondent Contact |
WILLIAM G MCMAHON |
Regulation Number | 892.1620
|
Classification Product Code |
|
Date Received | 02/21/1992 |
Decision Date | 07/17/1992 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Radiology
|
510k Review Panel |
Radiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|