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FDA 510(k)

BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237

K-Number: K081446 · 2008-07-17

ApplicantBecton, Dickinson & CO
Decision Date2008-07-17
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237 is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson & CO. It received FDA 510(k) clearance on 2008-07-17 under 510(k) number K081446. 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, MODELS: 405081, 405235, 405236, 405237?

BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237 is a medical device that received FDA 510(k) clearance on 2008-07-17. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K081446.

When did BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237 receive FDA 510(k) clearance?

BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237 received FDA 510(k) clearance on 2008-07-17, under 510(k) number K081446.

Who is the listed applicant for BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237?

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

What is the FDA product code for BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237?

The FDA product code for BD SPINAL NEEDLE, MODELS: 405081, 405235, 405236, 405237 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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