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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Spirometer, Diagnostic
510(k) Number K013123
Device Name EMS PULMONARY FUNCTION TESTING FILTER
Applicant
ENGINEERED MEDICAL SYSTEMS
6329 W. WATERVIEW CT.
MCCORDSVILLE,  IN  46055
Applicant Contact PAUL DRYDEN
Correspondent
ENGINEERED MEDICAL SYSTEMS
6329 W. WATERVIEW CT.
MCCORDSVILLE,  IN  46055
Correspondent Contact PAUL DRYDEN
Regulation Number868.1840
Classification Product Code
BZG  
Date Received09/19/2001
Decision Date 03/14/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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