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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 K884832
Device Name PERCUSSIONAIRE RESPIRATORS (MULTIPLE)
Applicant
Percussionaire Corp.
Bird Airlodge, Glengary Bay
P.O. Box 817
Sandpoint,  ID  83864
Applicant Contact BIRD, MD
Correspondent
Percussionaire Corp.
Bird Airlodge, Glengary Bay
P.O. Box 817
Sandpoint,  ID  83864
Correspondent Contact BIRD, MD
Regulation Number868.5895
Classification Product Code
CBK  
Date Received11/18/1988
Decision Date 09/14/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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