• 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 Stretcher, Wheeled
510(k) Number K952447
Device Name HILL-ROM AMBULATORY CARE PROCEDURAL STRETCHER
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 Number880.6910
Classification Product Code
FPO  
Date Received05/25/1995
Decision Date 11/22/1995
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
-
-