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FDA 510(k)

Flow-Nail

K-Number: K234075 · 2024-02-05

ApplicantFlow-Fx, LLC
Decision Date2024-02-05
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Flow-Nail is the device name listed in this FDA 510(k) record. The listed applicant is Flow-Fx, LLC. It received FDA 510(k) clearance on 2024-02-05 under 510(k) number K234075. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Flow-Nail?

Flow-Nail is a medical device that received FDA 510(k) clearance on 2024-02-05. The listed applicant is Flow-Fx, LLC. The 510(k) number is K234075.

When did Flow-Nail receive FDA 510(k) clearance?

Flow-Nail received FDA 510(k) clearance on 2024-02-05, under 510(k) number K234075.

Who is the listed applicant for Flow-Nail?

The FDA 510(k) record lists Flow-Fx, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Flow-Nail?

The FDA product code for Flow-Nail is HSB.

Other records listing Flow-Fx, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: HSB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.