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, Flotation Therapy, Powered
510(k) Number K945729
Device Name DYNAMICAIRE(TM) SLEEP SURFACE, ZONEAIR(TM) SLEEP SURFACE
Applicant
Hill-Rom, Inc.
1069 State Rte. 46 E.
Batesville,  IN  47006
Applicant Contact JAMES G CARPENTER
Correspondent
Hill-Rom, Inc.
1069 State Rte. 46 E.
Batesville,  IN  47006
Correspondent Contact JAMES G CARPENTER
Regulation Number890.5170
Classification Product Code
IOQ  
Date Received11/22/1994
Decision Date 02/27/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-