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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name calculator, predicted values, pulmonary function
510(k) Number K933839
Device Name MASTER SCREEN PNUEMO
Applicant
ERICH JAEGER, INC.
P.O. BOX 10008
ROCKFORD,  IL  61131
Applicant Contact A.G. KEIM
Correspondent
ERICH JAEGER, INC.
P.O. BOX 10008
ROCKFORD,  IL  61131
Correspondent Contact A.G. KEIM
Regulation Number868.1890
Classification Product Code
BTY  
Date Received08/05/1993
Decision Date 03/07/1994
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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