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 K030476
Device Name MODIFIED CONCENTRIC RETRIEVER, MODEL 90037
Applicant
CONCENTRIC MEDICAL, INC.
1380 SHOREBIRD WAY
MOUNTAIN VIEW,  CA 
Applicant Contact KEVIN F MACDONALD
Correspondent
CONCENTRIC MEDICAL, INC.
1380 SHOREBIRD WAY
MOUNTAIN VIEW,  CA 
Correspondent Contact KEVIN F MACDONALD
Regulation Number870.1250
Classification Product Code
DQY  
Date Received02/13/2003
Decision Date 03/11/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-