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 K873291
Device Name MSI 9000 SERIES BED
Applicant
Med Service, Inc.
P.O. Box 1296
Hwy. 6 W.
Batesville,  MS  38606
Applicant Contact BRUCE BAGGETT
Correspondent
Med Service, Inc.
P.O. Box 1296
Hwy. 6 W.
Batesville,  MS  38606
Correspondent Contact BRUCE BAGGETT
Regulation Number880.5100
Classification Product Code
FNL  
Date Received08/17/1987
Decision Date 12/30/1987
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
-
-