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 Pump, Infusion
510(k) Number K932847
Device Name CORPAK ENTERAL PUMP
Applicant
Corpak Co.
100 Chaddick Dr.
Wheeling,  IL  60090
Applicant Contact GEORGE NASSIF
Correspondent
Corpak Co.
100 Chaddick Dr.
Wheeling,  IL  60090
Correspondent Contact GEORGE NASSIF
Regulation Number880.5725
Classification Product Code
FRN  
Date Received06/10/1993
Decision Date 06/17/1994
Decision SE SUBJECT TO TRACKING REG (ST)
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
-
-