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FDA 510(k) Application Details - K013223
Device Classification Name
Generator, Oxygen, Portable
More FDA Info for this Device
510(K) Number
K013223
Device Name
Generator, Oxygen, Portable
Applicant
LITTON SYSTEMS, INC.
2734 HICKORY GROVE RD.
DAVENPORT, IA 52804-1203 US
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Contact
GARY BYRD
Other 510(k) Applications for this Contact
Regulation Number
868.5440
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Classification Product Code
CAW
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More FDA Info for this Product Code
Date Received
09/27/2001
Decision Date
02/11/2002
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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