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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact