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FDA 510(k), K013093, PALL ULTIPOR ANESTHESIA BREATHING SYSTEM
FDA 510(k), K013093, PALL ULTIPOR ANESTHESIA BREATHING SYSTEM
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510(K) Number: K013093
Device Name: PALL ULTIPOR ANESTHESIA BREATHING SYSTEM
Manufacturer: PALL MEDICAL
Device Classification Name: filter, bacterial, breathing-circuit
Regulation Number: 868.5260
Classification Product Code: CAH
Date Received: 09/17/2001
Decision Date: 08/01/2002
Regulation Medical Specialty: Anesthesiology
Device Name: PALL ULTIPOR ANESTHESIA BREATHING SYSTEM
Manufacturer: PALL MEDICAL
Device Classification Name: filter, bacterial, breathing-circuit
Regulation Number: 868.5260
Classification Product Code: CAH
Date Received: 09/17/2001
Decision Date: 08/01/2002
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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