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FDA 510(k) Applications Submitted by BARRY SMITH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K041348
05/20/2004
PORTEX ULTRAPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT_WITH SERIAL DILATORS OR SINGLE STAGE DILATOR, BLUE LINE ULTRA
SMITHS MEDICAL
K040014
12/24/2003
PERCUTANEOUS DILATION TRACHEOSTOMY KIT WITH SINGLE STAGE DILATOR AND SOFT INTRODUCERS FOR SIZES 7, 8 AND 9MM TUBES ONLY
PORTEX LTD.
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