FDA 510(k), K810893, HEWLETT-PACKARD VENTILATOR
FDA 510(k), K810893, HEWLETT-PACKARD VENTILATOR
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510(K) Number: K810893
Device Name: HEWLETT-PACKARD VENTILATOR
Manufacturer:
Device Classification Name: Ventilator, Continuous, Facility Use
Regulation Number: CBK
Classification Product Code: 04/02/1981
Date Received: 06/18/1981
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: HEWLETT-PACKARD VENTILATOR
Manufacturer:
Device Classification Name: Ventilator, Continuous, Facility Use
Regulation Number: CBK
Classification Product Code: 04/02/1981
Date Received: 06/18/1981
Decision Date: Substantially Equivalent (SESE)
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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