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FDA 510(k), K032226, LTV-1000 VENTILATOR
FDA 510(k), K032226, LTV-1000 VENTILATOR
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510(K) Number: K032226
Device Name: LTV-1000 VENTILATOR
Manufacturer: PULMONETIC SYSTEMS, INC.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 07/21/2003
Decision Date: 10/16/2003
Regulation Medical Specialty: Anesthesiology
Device Name: LTV-1000 VENTILATOR
Manufacturer: PULMONETIC SYSTEMS, INC.
Device Classification Name: ventilator, continuous, facility use
Regulation Number: 868.5895
Classification Product Code: CBK
Date Received: 07/21/2003
Decision Date: 10/16/2003
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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