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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 K880721
Device Name 6400ST INTERFACE MODULE-RS232
Original Applicant
BIRD PRODUCTS CORP.
1100 bird center dr.
palm springs,  CA  92262
Original Contact bentinck
Regulation Number868.5895
Classification Product Code
CBK  
Date Received02/23/1988
Decision Date 04/14/1988
Decision substantially equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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