VICROSAFE 6 AND VICROSAFE 12

Apparatus, Exhaust, Surgical

BUFFALO FILTER CO., INC.

The following data is part of a premarket notification filed by Buffalo Filter Co., Inc. with the FDA for Vicrosafe 6 And Vicrosafe 12.

Pre-market Notification Details

Device IDK930041
510k NumberK930041
Device Name:VICROSAFE 6 AND VICROSAFE 12
ClassificationApparatus, Exhaust, Surgical
Applicant BUFFALO FILTER CO., INC. 8388 BRIDLEWOOD DR. E. Amherst,  NY  14051
ContactClinton R Holland
CorrespondentClinton R Holland
BUFFALO FILTER CO., INC. 8388 BRIDLEWOOD DR. E. Amherst,  NY  14051
Product CodeFYD  
CFR Regulation Number878.5070 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-01-05
Decision Date1993-11-03

NIH GUDID Devices

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