• 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 Stand, Infusion
510(k) Number K850245
Device Name BREWER HEAVE-DUTY I.V. STAND W/FOOT OPERATED PNUEM
Applicant
E.F. Brewer Co.
13901 Main St.
P.O. Box 159
Menomonee Falls,  WI  53051
Applicant Contact RICHARD E ZIMMERMAN
Correspondent
E.F. Brewer Co.
13901 Main St.
P.O. Box 159
Menomonee Falls,  WI  53051
Correspondent Contact RICHARD E ZIMMERMAN
Regulation Number880.6990
Classification Product Code
FOX  
Date Received01/22/1985
Decision Date 02/07/1985
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
-
-