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FDA 510(k) Application Details - K972248
Device Classification Name
Ventilator, Continuous, Facility Use
More FDA Info for this Device
510(K) Number
K972248
Device Name
Ventilator, Continuous, Facility Use
Applicant
NELLCOR PURITAN BENNETT, INC.
10200 VALLEY VIEW RD.
EDEN PRAIRIE, MN 55344 US
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Contact
CHRIS HADLAND
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Regulation Number
868.5895
More FDA Info for this Regulation Number
Classification Product Code
CBK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/16/1997
Decision Date
09/12/1997
Decision
ST - Substantially Equivalent - Subject to Tracking Reg.
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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