FDA 510(k), K072290, PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUS
FDA 510(k), K072290, PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUS
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510(K) Number: K072290
Device Name: PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUS
Manufacturer: DIMA ITALIA SRL
Device Classification Name: ventilator, external body, negative pressure, adult (cuirass)
Regulation Number: 868.5935
Classification Product Code: BYT
Date Received: 08/16/2007
Decision Date: 05/29/2008
Regulation Medical Specialty: Anesthesiology
Device Name: PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUS
Manufacturer: DIMA ITALIA SRL
Device Classification Name: ventilator, external body, negative pressure, adult (cuirass)
Regulation Number: 868.5935
Classification Product Code: BYT
Date Received: 08/16/2007
Decision Date: 05/29/2008
Regulation Medical Specialty: Anesthesiology
- 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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