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 K990707
Device Name MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS
Applicant
Medtronics Interventional Vascular
37-A Cherry Hill Dr.
Danvers,  MA  01923
Applicant Contact MARK CHARTIER
Correspondent
Medtronics Interventional Vascular
37-A Cherry Hill Dr.
Danvers,  MA  01923
Correspondent Contact MARK CHARTIER
Regulation Number870.1250
Classification Product Code
DQY  
Date Received03/04/1999
Decision Date 03/22/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-