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FDA 510(k) Application Details - K955238
Device Classification Name
Stylet, Tracheal Tube
More FDA Info for this Device
510(K) Number
K955238
Device Name
Stylet, Tracheal Tube
Applicant
RUSCH INTL.
TALL PINES PARK
JAFFREY, NH 03452 US
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Contact
NEIL R ARMSTRONG
Other 510(k) Applications for this Contact
Regulation Number
868.5790
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Classification Product Code
BSR
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More FDA Info for this Product Code
Date Received
11/14/1995
Decision Date
02/06/1996
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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