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FDA 510(k) Application Details - K960795
Device Classification Name
Tube, Tracheal (W/Wo Connector)
More FDA Info for this Device
510(K) Number
K960795
Device Name
Tube, Tracheal (W/Wo Connector)
Applicant
VYGON CORP.
1129 BLOOMFIELD AVE.
WEST CALDWELL, NJ 07006 US
Other 510(k) Applications for this Company
Contact
ANNE MARIE CESARIO
Other 510(k) Applications for this Contact
Regulation Number
868.5730
More FDA Info for this Regulation Number
Classification Product Code
BTR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/27/1996
Decision Date
05/22/1996
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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