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FDA 510(k) Application Details - K945590
Device Classification Name
Laryngoscope, Rigid
More FDA Info for this Device
510(K) Number
K945590
Device Name
Laryngoscope, Rigid
Applicant
SMITH HELMS MULLISS & MOORE, L.L.P.
POST OFFICE BOX 21927
GREENSBORO, NC 27420 US
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Contact
CHRISTINE T NERO
Other 510(k) Applications for this Contact
Regulation Number
868.5540
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Classification Product Code
CCW
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More FDA Info for this Product Code
Date Received
11/14/1994
Decision Date
05/20/1997
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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