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FDA 510(k) Application Details - K983878
Device Classification Name
Bronchoscope (Flexible Or Rigid)
More FDA Info for this Device
510(K) Number
K983878
Device Name
Bronchoscope (Flexible Or Rigid)
Applicant
E. BENSON HOOD LABORATORIES, INC.
575 WASHINGTON ST.
PEMBROKE, MA 02359 US
Other 510(k) Applications for this Company
Contact
ANTHONY M SACCHETTI
Other 510(k) Applications for this Contact
Regulation Number
874.4680
More FDA Info for this Regulation Number
Classification Product Code
EOQ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/02/1998
Decision Date
01/29/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
EN - Ear, Nose, & Throat
Review Advisory Committee
EN - Ear, Nose, & Throat
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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