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FDA 510(k) Applications Submitted by Smiths Medical
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
K050166
01/26/2005
PORTEX EMERGENCY CRICOTHYROIDOTOMY KIT
SMITHS MEDICAL
K181660
06/25/2018
Acapella Choice Blue Vibratory PEP Device
Smiths Medical
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