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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