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FDA 510(k) Application Details - K990098
Device Classification Name
Tube, Tracheal (W/Wo Connector)
More FDA Info for this Device
510(K) Number
K990098
Device Name
Tube, Tracheal (W/Wo Connector)
Applicant
VENTLAB CORP.
PO BOX 4341
CROFTON, MD 21114-4341 US
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Contact
E J SMITH
Other 510(k) Applications for this Contact
Regulation Number
868.5730
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Classification Product Code
BTR
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More FDA Info for this Product Code
Date Received
01/12/1999
Decision Date
02/11/1999
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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