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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