• 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 chair, positioning, electric
510(k) Number K123834
Device Name EASYSTAND BANTAM MEDIUM
Applicant
ALTIMATE MEDICAL, INC.
262 WEST FIRST ST.
MORTON,  MN  56270
Applicant Contact STACEY FRANK
Correspondent
ALTIMATE MEDICAL, INC.
262 WEST FIRST ST.
MORTON,  MN  56270
Correspondent Contact STACEY FRANK
Regulation Number890.3110
Classification Product Code
INO  
Date Received12/13/2012
Decision Date 08/13/2013
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
-
-