FDA 510(k), K072002, FILTER CARESTAR 30; FILTER SAFESTAR 55; FILTER/HME TWINSTAR 55

FDA 510(k), K072002, FILTER CARESTAR 30; FILTER SAFESTAR 55; FILTER/HME TWINSTAR 55

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510(K) Number: K072002
Device Name: FILTER CARESTAR 30; FILTER SAFESTAR 55; FILTER/HME TWINSTAR 55
Manufacturer: DRAEGER MEDICAL AG & CO. KG
Device Classification Name: Filter, Bacterial, Breathing-Circuit
Regulation Number: 868.5260
Classification Product Code: CAH
Date Received: 07/23/2007
Decision Date: 01/31/2008
Regulation Medical Specialty: Anesthesiology
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