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FDA 510(k)

NinesMeasure

K-Number: K202990 · 2021-02-25

ApplicantNines, Inc.
Decision Date2021-02-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NinesMeasure is a medical device manufactured by Nines, Inc.. It received FDA 510(k) clearance on 2021-02-25 under approval number K202990. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NinesMeasure?

NinesMeasure is a medical device that received FDA 510(k) clearance on 2021-02-25. It is manufactured by Nines, Inc.. The 510(k) number is K202990.

When was NinesMeasure approved by the FDA?

NinesMeasure received FDA 510(k) clearance on 2021-02-25, under approval number K202990.

What company makes NinesMeasure?

NinesMeasure is manufactured by Nines, Inc..

What is the FDA product code for NinesMeasure?

The FDA product code for NinesMeasure is LLZ.

Other Devices by Nines, Inc.

K193351NinesAI

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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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