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FDA 510(k) Application Details - K990556
Device Classification Name
Tube, Tracheal (W/Wo Connector)
More FDA Info for this Device
510(K) Number
K990556
Device Name
Tube, Tracheal (W/Wo Connector)
Applicant
WOLFE TORY MEDICAL, INC.
79 WEST 4500 SOUTH, SUITE 21
SALT LAKE CITY, UT 84107 US
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Contact
TIM WOLFE
Other 510(k) Applications for this Contact
Regulation Number
868.5730
More FDA Info for this Regulation Number
Classification Product Code
BTR
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More FDA Info for this Product Code
Date Received
02/22/1999
Decision Date
03/26/1999
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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