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
Device Classification Name System, Tomographic, Nuclear
510(k) Number K832737
Device Name ECT PROCESSOR
Applicant
Siemens Gammasonics, Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Siemens Gammasonics, Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number892.1310
Classification Product Code
JWM  
Date Received08/11/1983
Decision Date 09/29/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-