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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 K001208
Device Name ESPIRT
Original Applicant
1501 ardmore blvd.
pittsburgh,  PA  15221 -4401
Original Contact kathy moore
Regulation Number868.5895
Classification Product Code
Date Received04/14/2000
Decision Date 05/12/2000
Decision substantially equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls