• 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 Wheelchair, Standup
510(k) Number K862305
Device Name ARISE, VIVRE DEBOUT
Applicant
Natco Corp.
1175 Chess Dr., Suite D
Foster City,  CA  94404
Applicant Contact BAXTER WATKINS
Correspondent
Natco Corp.
1175 Chess Dr., Suite D
Foster City,  CA  94404
Correspondent Contact BAXTER WATKINS
Regulation Number890.3900
Classification Product Code
IPL  
Date Received06/17/1986
Decision Date 07/09/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-