• 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, Powered
510(k) Number K000796
Device Name MAGIC MOBILITY 4 X 4 WHEELCHAIR
Applicant
VESTIL MANUFACTURING CORP.
900 GROWTH PKWY.
ANGOLA,  IN  46703
Applicant Contact RICK MICHAEL
Correspondent
VESTIL MANUFACTURING CORP.
900 GROWTH PKWY.
ANGOLA,  IN  46703
Correspondent Contact RICK MICHAEL
Regulation Number890.3860
Classification Product Code
ITI  
Date Received03/13/2000
Decision Date 08/11/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Abbreviated
Reviewed by Third Party No
Combination Product No
-
-