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FDA 510(k), K003075, KNIGHTSTAR 330 VENTILATOR
FDA 510(k), K003075, KNIGHTSTAR 330 VENTILATOR
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510(K) Number: K003075
Device Name: KNIGHTSTAR 330 VENTILATOR
Manufacturer: ANTHONY MULLIN
Device Classification Name: Ventilator, Continuous, Minimal Ventilatory Support, Facility Use
Regulation Number: MNT
Classification Product Code: KXA
Date Received: 10/03/2000
Decision Date: 12/11/2001
Decision Date: SE SUBJECT TO TRACKING REG (ST)
Regulation Medical Specialty: Anesthesiology
Device Name: KNIGHTSTAR 330 VENTILATOR
Manufacturer: ANTHONY MULLIN
Device Classification Name: Ventilator, Continuous, Minimal Ventilatory Support, Facility Use
Regulation Number: MNT
Classification Product Code: KXA
Date Received: 10/03/2000
Decision Date: 12/11/2001
Decision Date: SE SUBJECT TO TRACKING REG (ST)
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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