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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.
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