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 Device, Vascular, For Promoting Embolization
510(k) Number K151358
Device Name AZUR CX Detachable 35 Coils
Applicant
Microvention, Inc.
1311 Valencia Ave.
Tistin,  CA  92780
Applicant Contact Cynthia Valenzuela
Correspondent
Microvention, Inc.
1311 Valencia Ave.
Tistin,  CA  92780
Correspondent Contact Cynthia Valenzuela
Regulation Number870.3300
Classification Product Code
KRD  
Date Received05/20/2015
Decision Date 09/25/2015
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-