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FDA 510(k) Application Details - K984101
Device Classification Name
Laryngoscope, Rigid
More FDA Info for this Device
510(K) Number
K984101
Device Name
Laryngoscope, Rigid
Applicant
ARCO MEDIC LTD.
117 AHUZAH ST.
RA'ANANNA 43373 IL
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Contact
SHOSHANA FRIEDMAN
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
11/17/1998
Decision Date
09/03/1999
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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