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 Wheelchair, Powered
510(k) Number K904650
Device Name WHEELCHAIR CONVERSION KIT
Applicant
Hadco Marketing Services, Inc.
5601 Powerline Rd.
Suite 403
Ft. Lauderdale,  FL  33309
Applicant Contact ISAAC RODAN
Correspondent
Hadco Marketing Services, Inc.
5601 Powerline Rd.
Suite 403
Ft. Lauderdale,  FL  33309
Correspondent Contact ISAAC RODAN
Regulation Number890.3860
Classification Product Code
ITI  
Date Received10/02/1990
Decision Date 05/21/1991
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
-
-