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 Stretcher, Hand-Carried
510(k) Number K863686
Device Name BACK REST, LITTER, NON-ADJUSTABLE
Applicant
Brenner Metal Prod Corp.
16 Main Ave.
Wallington,  NJ  07057
Applicant Contact BRENNER, V.P.
Correspondent
Brenner Metal Prod Corp.
16 Main Ave.
Wallington,  NJ  07057
Correspondent Contact BRENNER, V.P.
Regulation Number880.6900
Classification Product Code
FPP  
Date Received09/19/1986
Decision Date 01/20/1987
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
-
-