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FDA 510(k), K011132, AIRLIFE HEPA FILTER
FDA 510(k), K011132, AIRLIFE HEPA FILTER
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510(K) Number: K011132
Device Name: AIRLIFE HEPA FILTER
Manufacturer: ALLEGIANCE HEALTHCARE CORP.
Device Classification Name: Filter, Bacterial, Breathing-Circuit
Regulation Number: 868.5260
Classification Product Code: CAH
Date Received: 04/13/2001
Decision Date: 06/08/2001
Regulation Medical Specialty: Anesthesiology
Device Name: AIRLIFE HEPA FILTER
Manufacturer: ALLEGIANCE HEALTHCARE CORP.
Device Classification Name: Filter, Bacterial, Breathing-Circuit
Regulation Number: 868.5260
Classification Product Code: CAH
Date Received: 04/13/2001
Decision Date: 06/08/2001
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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