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FDA 510(k) Application Details - K962736
Device Classification Name
Bronchoscope (Flexible Or Rigid)
More FDA Info for this Device
510(K) Number
K962736
Device Name
Bronchoscope (Flexible Or Rigid)
Applicant
MILL-ROSE LABORATORY
7310 CORPORATE BLVD.
MENTOR, OH 44060-4885 US
Other 510(k) Applications for this Company
Contact
ALAN C POJE
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
07/15/1996
Decision Date
07/29/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
EN - Ear, Nose, & Throat
Review Advisory Committee
EN - Ear, Nose, & Throat
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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