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 Set, Administration, Intravascular
510(k) Number K885031
Device Name LOW ADSORPTION ADMINISTRATION SET
Applicant
3M Company
1120 Red Fox Rd.
St. Paul,  MN  55112
Applicant Contact J SUEDKAMP
Correspondent
3M Company
1120 Red Fox Rd.
St. Paul,  MN  55112
Correspondent Contact J SUEDKAMP
Regulation Number880.5440
Classification Product Code
FPA  
Date Received12/05/1988
Decision Date 05/05/1989
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
-
-