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FDA 510(k) Application Details - K050153
Device Classification Name
Unit, Liquid-Oxygen, Portable
More FDA Info for this Device
510(K) Number
K050153
Device Name
Unit, Liquid-Oxygen, Portable
Applicant
CAIRE, INC.
1800 SANDY PLAINS INDUSTRIAL
PARKWAY, SUITE 316
MARIETTA, GA 30066 US
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Contact
DAN CHLAN
Other 510(k) Applications for this Contact
Regulation Number
868.5655
More FDA Info for this Regulation Number
Classification Product Code
BYJ
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More FDA Info for this Product Code
Date Received
01/24/2005
Decision Date
04/15/2005
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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