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 elevator, wheelchair, portable
510(k) Number K952946
Device Name VANGATOR II
Applicant
CROW RIVER INDUSTRIES, INC.
14800 28TH AVENUE NORTH
MINNEAPOLLIS,  MN  55447
Applicant Contact ROBERT C SAMEC
Correspondent
CROW RIVER INDUSTRIES, INC.
14800 28TH AVENUE NORTH
MINNEAPOLLIS,  MN  55447
Correspondent Contact ROBERT C SAMEC
Regulation Number890.3930
Classification Product Code
ING  
Date Received06/26/1995
Decision Date 11/29/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-