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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name ventilator, continuous, facility use
510(k) Number K001646
Device Name PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTION
Original Applicant
PURITAN BENNETT CORP.
2200 faraday ave.
carlsbad,  CA  92008
Original Contact mary e funk
Regulation Number868.5895
Classification Product Code
CBK  
Date Received05/30/2000
Decision Date 10/20/2000
Decision (ST)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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