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FDA 510(k), K103833, NEOPIP PATIENT CIRCUIT WITH PEEP
FDA 510(k), K103833, NEOPIP PATIENT CIRCUIT WITH PEEP
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510(K) Number: K103833
Device Name: NEOPIP PATIENT CIRCUIT WITH PEEP
Manufacturer: NEOFORCE GROUP, INC.
Device Classification Name: attachment, breathing, positive end expiratory pressure
Regulation Number: 868.5965
Classification Product Code: BYE
Date Received: 12/30/2010
Decision Date: 04/20/2011
Regulation Medical Specialty: Anesthesiology
Device Name: NEOPIP PATIENT CIRCUIT WITH PEEP
Manufacturer: NEOFORCE GROUP, INC.
Device Classification Name: attachment, breathing, positive end expiratory pressure
Regulation Number: 868.5965
Classification Product Code: BYE
Date Received: 12/30/2010
Decision Date: 04/20/2011
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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