FDA 510(k) Applications Submitted by CINDY ENGELHARDT

FDA 510(k) Number Submission Date Device Name Applicant
K110053 01/07/2011 CORRECTINJECT SAFETY SYSTEM, CATHETER CONNECTOR, FILTER, INFUSION ADAPTOR, SYRINGE KIT SMITHS MEDICAL ASD, INC.
K090261 02/03/2009 PORTEX TUOHY EPIDURAL NEEDLE 17G, PORTEX TUOHY EPIDURAL NEEDLE 18G SMITHS MEDICAL ASD, INC.
K092657 08/28/2009 EPIFUSE CATHETER CONNECTOR, MODEL: 4909E SMITHS MEDICAL ASD, 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.


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