FDA 510(k) Applications Submitted by PORTEX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K014073 12/10/2001 HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE PORTEX, INC.
K033080 09/29/2003 PORTEX 24G PEDIATRIC EPIDURAL AND PERIPHERAL BLOCK ANESTHESIA CATHETER PORTEX, INC.
K023793 11/13/2002 1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR PORTEX, INC.
K031057 04/03/2003 PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT PORTEX, INC.
K014115 12/14/2001 1ST RESPONSE MANUAL RESUSCITATOR, MODEL 85XX PORTEX, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact