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FDA 510(k), K092264, ATLANTIS HYPERBARIC CHAMBER VENTILATOR
FDA 510(k), K092264, ATLANTIS HYPERBARIC CHAMBER VENTILATOR
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$149.00 USD
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510(K) Number: K092264
Device Name: ATLANTIS HYPERBARIC CHAMBER VENTILATOR
Manufacturer: PROVIDENCE GLOBAL MEDICAL, INC.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 07/28/2009
Decision Date: 12/17/2009
Regulation Medical Specialty: Anesthesiology
Device Name: ATLANTIS HYPERBARIC CHAMBER VENTILATOR
Manufacturer: PROVIDENCE GLOBAL MEDICAL, INC.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 07/28/2009
Decision Date: 12/17/2009
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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