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FDA 510(k) Application Details - K022636
Device Classification Name
Plethysmograph, Volume
More FDA Info for this Device
510(K) Number
K022636
Device Name
Plethysmograph, Volume
Applicant
MORGAN SCIENTIFIC, INC.
151 ESSEX ST.
HAVERHILL, MA 01832 US
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Contact
PATRICK F MORGAN
Other 510(k) Applications for this Contact
Regulation Number
868.1760
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Classification Product Code
JEH
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More FDA Info for this Product Code
Date Received
08/08/2002
Decision Date
01/13/2003
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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