BD Syringe NRFit Lok and BD Syringe NRFit Slip
K-Number: K192538 · 2020-09-04
ApplicantBecton, Dickinson and Company
Decision Date2020-09-04
Product CodeQEH
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
BD Syringe NRFit Lok and BD Syringe NRFit Slip is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2020-09-04 under approval number K192538. The device is classified under product code QEH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BD Syringe NRFit Lok and BD Syringe NRFit Slip?
BD Syringe NRFit Lok and BD Syringe NRFit Slip is a medical device that received FDA 510(k) clearance on 2020-09-04. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K192538.
When was BD Syringe NRFit Lok and BD Syringe NRFit Slip approved by the FDA?
BD Syringe NRFit Lok and BD Syringe NRFit Slip received FDA 510(k) clearance on 2020-09-04, under approval number K192538.
What company makes BD Syringe NRFit Lok and BD Syringe NRFit Slip?
BD Syringe NRFit Lok and BD Syringe NRFit Slip is manufactured by Becton, Dickinson and Company.
What is the FDA product code for BD Syringe NRFit Lok and BD Syringe NRFit Slip?
The FDA product code for BD Syringe NRFit Lok and BD Syringe NRFit Slip is QEH.
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Related Devices (Code: QEH)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.