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FDA 510(k), K915075, NEBULIZER (DIRECT PATIENT INTERFACE)
FDA 510(k), K915075, NEBULIZER (DIRECT PATIENT INTERFACE)
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$149.00 USD
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510(K) Number: K915075
Device Name: NEBULIZER (DIRECT PATIENT INTERFACE)
Manufacturer: RUSSELL W.KING
Device Classification Name: Nebulizer (Direct Patient Interface)
Regulation Number: CAF
Classification Product Code: 11/08/1991
Date Received: 07/16/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: NEBULIZER (DIRECT PATIENT INTERFACE)
Manufacturer: RUSSELL W.KING
Device Classification Name: Nebulizer (Direct Patient Interface)
Regulation Number: CAF
Classification Product Code: 11/08/1991
Date Received: 07/16/1992
Decision Date: Substantially Equivalent (SESE)
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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