FDA 510(k), K163127, bellavista 1000
FDA 510(k), K163127, bellavista 1000
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510(K) Number: K163127
Device Name: bellavista 1000
Manufacturer: IMTMEDICAL AG
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 11/08/2016
Decision Date: 07/31/2017
Regulation Medical Specialty: Anesthesiology
Device Name: bellavista 1000
Manufacturer: IMTMEDICAL AG
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 11/08/2016
Decision Date: 07/31/2017
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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