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FDA 510(k) Application Details - K082600
Device Classification Name
Ventilator, Continuous, Facility Use
More FDA Info for this Device
510(K) Number
K082600
Device Name
Ventilator, Continuous, Facility Use
Applicant
DRAEGER MEDICAL B.V.
3135 Quarry Road
Telford, PA 18969 US
Other 510(k) Applications for this Company
Contact
JOYCE KILROY
Other 510(k) Applications for this Contact
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
09/08/2008
Decision Date
11/26/2008
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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