FDA 510(k), K041623, REUSABLE STERILCONTAINER FILTER MODEL #JK090
FDA 510(k), K041623, REUSABLE STERILCONTAINER FILTER MODEL #JK090
Device Name: REUSABLE STERILCONTAINER FILTER MODEL #JK090
Manufacturer:
Device Classification Name: Wrap, Sterilization
Regulation Number: 880.6850
Classification Product Code: FRG
Date Received: 06/16/2004
Decision Date: 12/13/2004
Regulation Medical Specialty: General Hospital
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