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 K881410
Device Name THE ADVENTURER
Applicant
Westport Mobility Products, Inc.
P.O. Box 248
Westport, Ontario
Canada,  CA K0G 1X0
Applicant Contact HERB WESTCOTT
Correspondent
Westport Mobility Products, Inc.
P.O. Box 248
Westport, Ontario
Canada,  CA K0G 1X0
Correspondent Contact HERB WESTCOTT
Regulation Number890.3850
Classification Product Code
IOR  
Date Received04/04/1988
Decision Date 04/21/1988
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
-
-