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FDA 510(k)

BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle

K-Number: K210978 · 2021-12-22

ApplicantBecton, Dickinson and Company
Decision Date2021-12-22
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2021-12-22 under approval number K210978. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle?

BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle is a medical device that received FDA 510(k) clearance on 2021-12-22. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K210978.

When was BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle approved by the FDA?

BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle received FDA 510(k) clearance on 2021-12-22, under approval number K210978.

What company makes BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle?

BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle?

The FDA product code for BD Quincke Spinal Needle, BD Whitacre Spinal Needle, BD Spinal Introducer Needle is BSP.

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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.

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