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 Implantable Pacemaker Pulse-Generator
510(k) Number K894240
Device Name NEOS 02
Applicant
Biotronik Cardiac Pacemakers
P.O. Box 1988
Lake Oswego,  CA  97034
Applicant Contact RICHARD STOUT
Correspondent
Biotronik Cardiac Pacemakers
P.O. Box 1988
Lake Oswego,  CA  97034
Correspondent Contact RICHARD STOUT
Regulation Number870.3610
Classification Product Code
DXY  
Date Received06/20/1989
Decision Date 10/26/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-