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FDA 510(k), K830009, OXYMIZER
FDA 510(k), K830009, OXYMIZER
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510(K) Number: K830009
Device Name: OXYMIZER
Manufacturer:
Device Classification Name: Conserver, Oxygen
Regulation Number: NFB
Classification Product Code: 01/03/1983
Date Received: 04/02/1983
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: OXYMIZER
Manufacturer:
Device Classification Name: Conserver, Oxygen
Regulation Number: NFB
Classification Product Code: 01/03/1983
Date Received: 04/02/1983
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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