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 Bed, Ac-Powered Adjustable Hospital
510(k) Number K911893
Device Name EASY ACCESS BED
Applicant
Willis Therapeutic Innovations, Inc.
P.O.Box 184
Westhampton Beach,  NY  11978
Applicant Contact WILLIAM WILLIS
Correspondent
Willis Therapeutic Innovations, Inc.
P.O.Box 184
Westhampton Beach,  NY  11978
Correspondent Contact WILLIAM WILLIS
Regulation Number880.5100
Classification Product Code
FNL  
Date Received04/29/1991
Decision Date 11/22/1991
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
-
-