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FDA 510(k)

TRUEdraw Lancing Device, Mini Lancing Device

K-Number: K221072 · 2022-10-18

ApplicantTrividia Health
Decision Date2022-10-18
Product CodeQRL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRUEdraw Lancing Device, Mini Lancing Device is a medical device manufactured by Trividia Health. It received FDA 510(k) clearance on 2022-10-18 under approval number K221072. The device is classified under product code QRL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRUEdraw Lancing Device, Mini Lancing Device?

TRUEdraw Lancing Device, Mini Lancing Device is a medical device that received FDA 510(k) clearance on 2022-10-18. It is manufactured by Trividia Health. The 510(k) number is K221072.

When was TRUEdraw Lancing Device, Mini Lancing Device approved by the FDA?

TRUEdraw Lancing Device, Mini Lancing Device received FDA 510(k) clearance on 2022-10-18, under approval number K221072.

What company makes TRUEdraw Lancing Device, Mini Lancing Device?

TRUEdraw Lancing Device, Mini Lancing Device is manufactured by Trividia Health.

What is the FDA product code for TRUEdraw Lancing Device, Mini Lancing Device?

The FDA product code for TRUEdraw Lancing Device, Mini Lancing Device is QRL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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