• 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 K102061
Device Name TREVAIR CHAIR ADULT
Applicant
Patmont Motor Werks, Inc.
2220 Meridian Blvd.
Minden,  NV  89423
Applicant Contact STEVEN J PATMONT
Correspondent
Patmont Motor Werks, Inc.
2220 Meridian Blvd.
Minden,  NV  89423
Correspondent Contact STEVEN J PATMONT
Regulation Number890.3850
Classification Product Code
IOR  
Date Received07/22/2010
Decision Date 12/13/2010
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
Predetermined Change
Control Plan Authorized
No
-
-