• 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 Lift, Patient, Ac-Powered
510(k) Number K926411
Device Name SAF-LIFT/SAF-KARY
Applicant
Arjo-Century, Inc.
Industrial Park
Aurora,  NE  68818
Applicant Contact JAMES L KADOW
Correspondent
Arjo-Century, Inc.
Industrial Park
Aurora,  NE  68818
Correspondent Contact JAMES L KADOW
Regulation Number880.5500
Classification Product Code
FNG  
Date Received12/21/1992
Decision Date 03/31/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-