Blood Specimen Collection Devices - Vacuum

Tubes, Vials, Systems, Serum Separators, Blood Collection

Becton, Dickinson & Company

The following data is part of a premarket notification filed by Becton, Dickinson & Company with the FDA for Blood Specimen Collection Devices - Vacuum.

Pre-market Notification Details

Device IDBK050036
510k NumberBK050036
Device Name:Blood Specimen Collection Devices - Vacuum
ClassificationTubes, Vials, Systems, Serum Separators, Blood Collection
Applicant Becton, Dickinson & Company 1 Becton Drive, Mc 300 Franklin Lakes,  NJ  07417
Product CodeJKA  
CFR Regulation Number862.1675 [🔎]
DecisionSubstantially Equivalent (SE)
Type510(k) Traditio
3rd Party ReviewedNo
Combination ProductNo
Date Received2005-06-24
Decision Date2006-02-24

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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