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FDA 510(k), K032922, CLARISSA INFANT NCPAP CANNULA
FDA 510(k), K032922, CLARISSA INFANT NCPAP CANNULA
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510(K) Number: K032922
Device Name: CLARISSA INFANT NCPAP CANNULA
Manufacturer: AIRWAYS LTD., INC.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 09/22/2003
Decision Date: 09/22/2004
Regulation Medical Specialty: Anesthesiology
Device Name: CLARISSA INFANT NCPAP CANNULA
Manufacturer: AIRWAYS LTD., INC.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 09/22/2003
Decision Date: 09/22/2004
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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