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FDA 510(k)

Neurophet AQUA

K-Number: K220437 · 2023-05-10

ApplicantNeurophet., Inc.
Decision Date2023-05-10
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Neurophet AQUA is a medical device manufactured by Neurophet., Inc.. It received FDA 510(k) clearance on 2023-05-10 under approval number K220437. 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 Neurophet AQUA?

Neurophet AQUA is a medical device that received FDA 510(k) clearance on 2023-05-10. It is manufactured by Neurophet., Inc.. The 510(k) number is K220437.

When was Neurophet AQUA approved by the FDA?

Neurophet AQUA received FDA 510(k) clearance on 2023-05-10, under approval number K220437.

What company makes Neurophet AQUA?

Neurophet AQUA is manufactured by Neurophet., Inc..

What is the FDA product code for Neurophet AQUA?

The FDA product code for Neurophet AQUA is LLZ.

Other Devices by Neurophet., Inc.

K221405Neurophet SCALE PET K242215Neurophet AQUA (V3.1) K252563Neurophet SCALE PET K261273Neurophet AQUA K252496Neurophet AQUA AD Plus

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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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