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 Catheter, Straight
510(k) Number K030538
Device Name AMERICAN CATHETER, MODEL W3
Applicant
CATHETER LLC.
106 GROPPO DR.
WINSTED,  CT  06098 -0917
Applicant Contact JOHN C DEVANNEY
Correspondent
CATHETER LLC.
106 GROPPO DR.
WINSTED,  CT  06098 -0917
Correspondent Contact JOHN C DEVANNEY
Regulation Number876.5130
Classification Product Code
EZD  
Date Received02/20/2003
Decision Date 03/10/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-