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FDA 510(k), K172335, Bleep DreamPort
FDA 510(k), K172335, Bleep DreamPort
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$149.00 USD
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510(K) Number: K172335
Device Name: Bleep DreamPort
Manufacturer: Stuart Heatherington
Device Classification Name: Ventilator, Non-Continuous (Respirator)
Regulation Number: BZD
Classification Product Code: 08/02/2017
Date Received: 03/30/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: Bleep DreamPort
Manufacturer: Stuart Heatherington
Device Classification Name: Ventilator, Non-Continuous (Respirator)
Regulation Number: BZD
Classification Product Code: 08/02/2017
Date Received: 03/30/2018
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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