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FDA 510(k) Application Details - K971129
Device Classification Name
Generator, Oxygen, Portable
More FDA Info for this Device
510(K) Number
K971129
Device Name
Generator, Oxygen, Portable
Applicant
ARBOR RESEARCH CORP.
806 AIRPORT BLVD.
ANN ARBOR, MI 48108 US
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Contact
BLAKE M PATERSON
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
03/27/1997
Decision Date
06/24/1997
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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