• 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 Catheter And Tip, Suction
510(k) Number K873464
Device Name VAN DELLEN CANNULA
Applicant
VAN DELLEN, LTD.
3810 E. 44TH ST., SUITE 301
P.O. BOX 27748
TUCSON,  AZ  85726
Applicant Contact ROGER DANHOF
Correspondent
VAN DELLEN, LTD.
3810 E. 44TH ST., SUITE 301
P.O. BOX 27748
TUCSON,  AZ  85726
Correspondent Contact ROGER DANHOF
Regulation Number880.6740
Classification Product Code
JOL  
Date Received08/28/1987
Decision Date 11/23/1987
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
-
-