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, Planning, Radiation Therapy Treatment
510(k) Number K012017
Device Name VARISEED 7.0
Applicant
Varian Medical Systems
3100 Hansen Way
Palo Alto,  CA  94304 -1129
Applicant Contact LINDA S NASH
Correspondent
Varian Medical Systems
3100 Hansen Way
Palo Alto,  CA  94304 -1129
Correspondent Contact LINDA S NASH
Regulation Number892.5050
Classification Product Code
MUJ  
Date Received06/28/2001
Decision Date 07/12/2001
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-