FDA 510(k), K140799, CELERITY SYSYEM

FDA 510(k), K140799, CELERITY SYSYEM

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510(K) Number: K140799
Device Name: CELERITY SYSYEM
Manufacturer: Lorraine M Hanley
Device Classification Name: Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Regulation Number: LJS
Classification Product Code: 03/31/2014
Date Received: 06/13/2014
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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