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FDA 510(k), K161454, Propeller Sensor Model 2015-E
FDA 510(k), K161454, Propeller Sensor Model 2015-E
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510(K) Number: K161454
Device Name: Propeller Sensor Model 2015-E
Manufacturer: Taylor Mahan-Rudolph
Device Classification Name: Nebulizer (Direct Patient Interface)
Regulation Number: CAF
Classification Product Code: 05/26/2016
Date Received: 11/01/2016
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: Propeller Sensor Model 2015-E
Manufacturer: Taylor Mahan-Rudolph
Device Classification Name: Nebulizer (Direct Patient Interface)
Regulation Number: CAF
Classification Product Code: 05/26/2016
Date Received: 11/01/2016
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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