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 K940446
Device Name 3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION)
Applicant
MINNESOTA MINING AND MFG. CO.
3M CENTER, BUILDING 275-3E-08
P.O. BOX 33275
ST. PAUL,  MN  55133 -3275
Applicant Contact DOROTHEA VON BUSCH
Correspondent
MINNESOTA MINING AND MFG. CO.
3M CENTER, BUILDING 275-3E-08
P.O. BOX 33275
ST. PAUL,  MN  55133 -3275
Correspondent Contact DOROTHEA VON BUSCH
Regulation Number880.5725
Classification Product Code
FRN  
Date Received02/01/1994
Decision Date 08/15/1994
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
Recalls CDRH Recalls
-
-