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FDA 510(k) Application Details - K011329
Device Classification Name
Rhinoanemometer (Measurement Of Nasal Decongestion)
More FDA Info for this Device
510(K) Number
K011329
Device Name
Rhinoanemometer (Measurement Of Nasal Decongestion)
Applicant
E. BENSON HOOD LAB, INC.
575 WASHINGTON ST.
PEMBROKE, MA 02359 US
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Contact
LEWIS MARTEN
Other 510(k) Applications for this Contact
Regulation Number
868.1800
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Classification Product Code
BXQ
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More FDA Info for this Product Code
Date Received
05/01/2001
Decision Date
07/26/2002
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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