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, Intravascular Occluding, Temporary
510(k) Number K210602
Device Name AortaSTAT Occlusion Device
Applicant
Renalpro Medical, Inc.
2370-B Walsh Ave.
Santa Clara,  CA  95051
Applicant Contact James Twitchell
Correspondent
Northwest Clinical Research Group, Inc.
19836 NE 125th Pl.
Woodinville,  WA  98077
Correspondent Contact Roberta Hines
Regulation Number870.4450
Classification Product Code
MJN  
Date Received03/01/2021
Decision Date 07/09/2021
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
-
-