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FDA 510(k), K811409, ARGYLE CPAP NASAL CANNULA
FDA 510(k), K811409, ARGYLE CPAP NASAL CANNULA
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510(K) Number: K811409
Device Name: ARGYLE CPAP NASAL CANNULA
Manufacturer: SHERWOOD MEDICAL CO.
Device Classification Name: ventilator, non-continuous (respirator)
Regulation Number: 868.5905
Classification Product Code: BZD
Date Received: 05/19/1981
Decision Date: 06/02/1981
Regulation Medical Specialty: Anesthesiology
Device Name: ARGYLE CPAP NASAL CANNULA
Manufacturer: SHERWOOD MEDICAL CO.
Device Classification Name: ventilator, non-continuous (respirator)
Regulation Number: 868.5905
Classification Product Code: BZD
Date Received: 05/19/1981
Decision Date: 06/02/1981
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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