FDA 510(k) Application Details - K021200

Device Classification Name Spirometer, Diagnostic

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510(K) Number K021200
Device Name Spirometer, Diagnostic
Applicant MORGAN SCIENTIFIC, INC.
151 ESSEX ST.
HAVERHILL, MA 01832 US
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Contact PATRICK F MORGAN
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Regulation Number 868.1840

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Classification Product Code BZG
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Date Received 04/16/2002
Decision Date 10/18/2002
Decision SESE - SUBST EQUIV
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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