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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 K993071
Device Name PURITAN-BENNETT VENTILATOR SYSTEM WITH ET/TRACHEOSTOMY TUBE COMPENSATION, TC, OPTION, MODEL 840
Original Applicant
PURITAN BENNETT CORP.
2200 faraday ave.
carlsbad,  CA  92008
Original Contact delton west
Regulation Number868.5895
Classification Product Code
CBK  
Date Received09/14/1999
Decision Date 11/24/1999
Decision (ST)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
summary summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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