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FDA 510(k)

BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle

K-Number: K211085 · 2022-07-01

ApplicantBecton, Dickinson and Company
Decision Date2022-07-01
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2022-07-01 under 510(k) number K211085. 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 Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle?

BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle is a medical device that received FDA 510(k) clearance on 2022-07-01. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K211085.

When did BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle receive FDA 510(k) clearance?

BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle received FDA 510(k) clearance on 2022-07-01, under 510(k) number K211085.

Who is the listed applicant for BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle?

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

What is the FDA product code for BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural Needle?

The FDA product code for BD Perisafe Tuohy Epidural Needle, BD Perisafe Weiss Epidural 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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