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 Cable, Transducer And Electrode, Patient, (Including Connector)
510(k) Number K901780
Device Name RTM 36-05, 60-05, RTD 36-05, 60-05 RADIO. LEADWIRE
Applicant
Medtronic Vascular
60 Newark St.
Haverhill,  MA  01830
Applicant Contact JANICE M PEVIDE
Correspondent
Medtronic Vascular
60 Newark St.
Haverhill,  MA  01830
Correspondent Contact JANICE M PEVIDE
Regulation Number870.2900
Classification Product Code
DSA  
Date Received04/17/1990
Decision Date 10/09/1990
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
-
-