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FDA 510(k) Application Details - K000904
Device Classification Name
Apparatus, Exhaust, Surgical
More FDA Info for this Device
510(K) Number
K000904
Device Name
Apparatus, Exhaust, Surgical
Applicant
BUFFALO FILTER CO., INC.
595 COMMERCE DR.
BUFFALO, NY 14228 US
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Contact
KATHLEEN H SELOVER
Other 510(k) Applications for this Contact
Regulation Number
878.5070
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Classification Product Code
FYD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/21/2000
Decision Date
06/08/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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