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FDA 510(k), K132021, AHP 300, EMERGENCY PORTABLE VENTILATOR
FDA 510(k), K132021, AHP 300, EMERGENCY PORTABLE VENTILATOR
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510(K) Number: K132021
Device Name: AHP 300, EMERGENCY PORTABLE VENTILATOR
Manufacturer: ALLIED HEALTHCARE PRODUCTS, INC.
Device Classification Name: ventilator, emergency, powered (resuscitator)
Regulation Number: 868.5925
Classification Product Code: BTL
Date Received: 07/02/2013
Decision Date: 04/02/2014
Regulation Medical Specialty: Anesthesiology
Device Name: AHP 300, EMERGENCY PORTABLE VENTILATOR
Manufacturer: ALLIED HEALTHCARE PRODUCTS, INC.
Device Classification Name: ventilator, emergency, powered (resuscitator)
Regulation Number: 868.5925
Classification Product Code: BTL
Date Received: 07/02/2013
Decision Date: 04/02/2014
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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