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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name meter, peak flow, spirometry
510(k) Number K924343
Device Name WRIGHT POCKET PEAK FLOW METER
Applicant
FERRARIS MEDICAL, INC.
P.O. BOX 344
HOLLAND,  NY  14080
Applicant Contact DAVID R MALYS
Correspondent
FERRARIS MEDICAL, INC.
P.O. BOX 344
HOLLAND,  NY  14080
Correspondent Contact DAVID R MALYS
Regulation Number868.1860
Classification Product Code
BZH  
Date Received08/27/1992
Decision Date 06/16/1993
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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