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 Catheter, Percutaneous
510(k) Number K022764
Device Name 7F LAUNCHER GUIDE CATHETER
Applicant
MEDTRONIC VASCULAR
37A CHERRY HILL DR.
DANVERS,  MA  01923
Applicant Contact FRED L BOUCHER
Correspondent
MEDTRONIC VASCULAR
37A CHERRY HILL DR.
DANVERS,  MA  01923
Correspondent Contact FRED L BOUCHER
Regulation Number870.1250
Classification Product Code
DQY  
Date Received08/21/2002
Decision Date 08/28/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
-
-