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FDA 510(k), K173181, ExSpiron 1Xi
FDA 510(k), K173181, ExSpiron 1Xi
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510(K) Number: K173181
Device Name: ExSpiron 1Xi
Manufacturer: Susan Hamann
Device Classification Name: Spirometer, Monitoring (W/Wo Alarm)
Regulation Number: BZK
Classification Product Code: 09/29/2017
Date Received: 03/16/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: ExSpiron 1Xi
Manufacturer: Susan Hamann
Device Classification Name: Spirometer, Monitoring (W/Wo Alarm)
Regulation Number: BZK
Classification Product Code: 09/29/2017
Date Received: 03/16/2018
Decision Date: Substantially Equivalent (SESE)
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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