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FDA 510(k), K091459, PHILIPS NM3 MONITOR, MODEL 7900
FDA 510(k), K091459, PHILIPS NM3 MONITOR, MODEL 7900
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510(K) Number: K091459
Device Name: PHILIPS NM3 MONITOR, MODEL 7900
Manufacturer: RESPIRONICS NOVAMETRIX LLC
Device Classification Name: Spirometer, Monitoring (W/Wo Alarm)
Regulation Number: 868.1850
Classification Product Code: BZK
Date Received: 05/18/2009
Decision Date: 07/28/2009
Regulation Medical Specialty: Anesthesiology
Device Name: PHILIPS NM3 MONITOR, MODEL 7900
Manufacturer: RESPIRONICS NOVAMETRIX LLC
Device Classification Name: Spirometer, Monitoring (W/Wo Alarm)
Regulation Number: 868.1850
Classification Product Code: BZK
Date Received: 05/18/2009
Decision Date: 07/28/2009
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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