• 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, irrigation
510(k) Number K950437
Device Name ANGIOCATH SIDEHOLDER DRAINAGE CATHETER
Applicant
BECTON DICKINSON VASCULAR ACCESS, INC.
9450 SOUTH STATE ST.
SANDY,  UT  84070
Applicant Contact C. J WELLE
Correspondent
BECTON DICKINSON VASCULAR ACCESS, INC.
9450 SOUTH STATE ST.
SANDY,  UT  84070
Correspondent Contact C. J WELLE
Regulation Number878.4200
Classification Product Code
GBX  
Date Received02/02/1995
Decision Date 03/14/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-