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, mechanical
510(k) Number K063736
Device Name FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50
Applicant
PDG PRODUCT DESIGN GROUP, INC.
5905 FAWN LANE
CLEVELAND,  OH  44141
Applicant Contact EDWARD A KROLL
Correspondent
PDG PRODUCT DESIGN GROUP, INC.
5905 FAWN LANE
CLEVELAND,  OH  44141
Correspondent Contact EDWARD A KROLL
Regulation Number890.3850
Classification Product Code
IOR  
Date Received12/18/2006
Decision Date 01/17/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-