Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
510(k) Number K828564
Device Name COMPUTER DATA MONITORING SYSTEM
Applicant
Siemens Medical Solutions USA, Inc.
22010 SE 51st St.
Issaquah,  WA  98027
Correspondent
Siemens Medical Solutions USA, Inc.
22010 SE 51st St.
Issaquah,  WA  98027
Date Received10/08/1982
Decision Date 01/03/1983
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-