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 Needle, Hypodermic, Single Lumen
510(k) Number K861390
Device Name DEPTH MEASURING NEEDLES/VASCU IMPLANT ACCESS SET
Applicant
Baxter Healthcare Corp
Londonderry Tpke.
Hooksett,  NH  03104
Applicant Contact ROGER A LEROUX
Correspondent
Baxter Healthcare Corp
Londonderry Tpke.
Hooksett,  NH  03104
Correspondent Contact ROGER A LEROUX
Regulation Number880.5570
Classification Product Code
FMI  
Date Received04/14/1986
Decision Date 07/17/1986
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
-
-