• 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 Pump, Infusion
510(k) Number K850098
Device Name SILVER SPOON ENTERAL FEEDING PUMP
Applicant
Sterling Medical Devices, Inc.
1616 W. Shaw Ave.
Suite D-1
Fresno,  CA  93711
Applicant Contact FRANK FERGUSON
Correspondent
Sterling Medical Devices, Inc.
1616 W. Shaw Ave.
Suite D-1
Fresno,  CA  93711
Correspondent Contact FRANK FERGUSON
Regulation Number880.5725
Classification Product Code
FRN  
Date Received01/11/1985
Decision Date 02/22/1985
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
-
-