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FDA 510(k), K171899, Revitalair 430F
FDA 510(k), K171899, Revitalair 430F
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$149.00 USD
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510(K) Number: K171899
Device Name: Revitalair 430F
Manufacturer: Oxavita S.R.L.
Device Classification Name: Chamber, Hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 06/26/2017
Decision Date: 11/22/2019
Regulation Medical Specialty: Anesthesiology
Device Name: Revitalair 430F
Manufacturer: Oxavita S.R.L.
Device Classification Name: Chamber, Hyperbaric
Regulation Number: 868.5470
Classification Product Code: CBF
Date Received: 06/26/2017
Decision Date: 11/22/2019
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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