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 K934090
Device Name S.S.C. MEDICAL MODEL 5000 SERIES BED
Applicant
Super Sagless Corp.
1691 S. Green St.
P.O. Box 197
Tupelo,  MS  38802
Applicant Contact JEFFREY L PLUNK
Correspondent
Super Sagless Corp.
1691 S. Green St.
P.O. Box 197
Tupelo,  MS  38802
Correspondent Contact JEFFREY L PLUNK
Regulation Number880.5100
Classification Product Code
FNL  
Date Received08/24/1993
Decision Date 02/09/1994
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
-
-