• 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 clip, implantable
510(k) Number K020879
Device Name IVS CLIP CLOSURE SYSTEM, MODEL 1002 (IVS CLIP APPLIER); IVS INTRUDUCER SET, MODEL 1001
Applicant
INTEGRATED VASCULAR SYSTEMS, INC.
743 NORTH PASTORIA AVE.
SUNNYVALE,  CA  94085
Applicant Contact SUSAN TURNER
Correspondent
INTEGRATED VASCULAR SYSTEMS, INC.
743 NORTH PASTORIA AVE.
SUNNYVALE,  CA  94085
Correspondent Contact SUSAN TURNER
Regulation Number878.4300
Classification Product Code
FZP  
Date Received03/18/2002
Decision Date 09/25/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-