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FDA 510(k) Application Details - K020280
Device Classification Name
Spirometer, Diagnostic
More FDA Info for this Device
510(K) Number
K020280
Device Name
Spirometer, Diagnostic
Applicant
MORGAN MEDICAL LTD.
555 THIRTEENTH ST. NW
WASHINGTON, DC 20004-1109 US
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Contact
JONATHAN S KAHAN
Other 510(k) Applications for this Contact
Regulation Number
868.1840
More FDA Info for this Regulation Number
Classification Product Code
BZG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/28/2002
Decision Date
09/24/2002
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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