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 K872925
Device Name MEGABED 1000
Applicant
Surgi-Med, Inc.
815 Terminal Rd.
Lansing,  MI  48906
Applicant Contact DONALD J PROPP
Correspondent
Surgi-Med, Inc.
815 Terminal Rd.
Lansing,  MI  48906
Correspondent Contact DONALD J PROPP
Regulation Number880.5100
Classification Product Code
FNL  
Date Received07/27/1987
Decision Date 09/15/1987
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
-
-