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 Lift, Patient, Ac-Powered
510(k) Number K896848
Device Name LIFT MASTER PATIENT LIFT
Applicant
Henry Enterprises, Inc.
P.O. Box 24
Concordia,  KS  66901
Applicant Contact BARBARA J HENRY
Correspondent
Henry Enterprises, Inc.
P.O. Box 24
Concordia,  KS  66901
Correspondent Contact BARBARA J HENRY
Regulation Number880.5500
Classification Product Code
FNG  
Date Received12/05/1989
Decision Date 05/29/1990
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
-
-