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FDA 510(k)

BD SPINAL NEEDLE 27G

K-Number: K091758 · 2009-10-09

ApplicantBecton Dickson & Co.
Decision Date2009-10-09
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BD SPINAL NEEDLE 27G is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickson & Co.. It received FDA 510(k) clearance on 2009-10-09 under 510(k) number K091758. 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 SPINAL NEEDLE 27G?

BD SPINAL NEEDLE 27G is a medical device that received FDA 510(k) clearance on 2009-10-09. The listed applicant is Becton Dickson & Co.. The 510(k) number is K091758.

When did BD SPINAL NEEDLE 27G receive FDA 510(k) clearance?

BD SPINAL NEEDLE 27G received FDA 510(k) clearance on 2009-10-09, under 510(k) number K091758.

Who is the listed applicant for BD SPINAL NEEDLE 27G?

The FDA 510(k) record lists Becton Dickson & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD SPINAL NEEDLE 27G?

The FDA product code for BD SPINAL NEEDLE 27G 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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