Device Classification Name |
solid state x-ray imager (flat panel/digital imager)
|
510(k) Number |
K202564 |
Device Name |
DigitalDiagnost C90 |
Applicant |
Philips Medical Systems DMC GmbH |
Röntgenstraße 24 |
Hamburg,
DE
22335
|
|
Applicant Contact |
Ming Xiao |
Correspondent |
REGULATORY TECHNOLOGY SERVICES, LLC |
1000 Westgate Drive, |
Suite 510k |
Saint Paul,
MN
55114
|
|
Correspondent Contact |
Prithul Bom |
Regulation Number | 892.1680
|
Classification Product Code |
|
Subsequent Product Codes |
|
Date Received | 09/04/2020 |
Decision Date | 09/30/2020 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Radiology
|
510k Review Panel |
Radiology
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
Yes
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|