FDA 510(k), K142541, POCKET NEB
FDA 510(k), K142541, POCKET NEB
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510(K) Number: K142541
Device Name: POCKET NEB
Manufacturer: MicroVaper Devices
Device Classification Name: nebulizer (direct patient interface)
Regulation Number: 868.5630
Classification Product Code: CAF
Date Received: 09/10/2014
Decision Date: 01/22/2016
Regulation Medical Specialty: Anesthesiology
Device Name: POCKET NEB
Manufacturer: MicroVaper Devices
Device Classification Name: nebulizer (direct patient interface)
Regulation Number: 868.5630
Classification Product Code: CAF
Date Received: 09/10/2014
Decision Date: 01/22/2016
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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