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 Clamp, Vascular
510(k) Number K891296
Device Name ATRAUMAX(TM) SURGICAL CLAMPS
Applicant
Applied Vascular Devices, Inc.
2740 S. Harbor, Suite K
Santa Ana,  CA  92704
Applicant Contact SAID S HILAL
Correspondent
Applied Vascular Devices, Inc.
2740 S. Harbor, Suite K
Santa Ana,  CA  92704
Correspondent Contact SAID S HILAL
Regulation Number870.4450
Classification Product Code
DXC  
Date Received03/13/1989
Decision Date 06/07/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-