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FDA 510(k)

BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets

K-Number: K223243 · 2022-12-16

ApplicantBecton, Dickinson and Company
Decision Date2022-12-16
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2022-12-16 under approval number K223243. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets?

BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets is a medical device that received FDA 510(k) clearance on 2022-12-16. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K223243.

When was BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets approved by the FDA?

BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets received FDA 510(k) clearance on 2022-12-16, under approval number K223243.

What company makes BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets?

BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets?

The FDA product code for BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel™ Lancets is FMK.

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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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