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FDA 510(k)

PliaFX Flo

K-Number: K242799 · 2024-11-21

ApplicantLifenet Health
Decision Date2024-11-21
Product CodeMBP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PliaFX Flo is the device name listed in this FDA 510(k) record. The listed applicant is Lifenet Health. It received FDA 510(k) clearance on 2024-11-21 under 510(k) number K242799. The device is classified under product code MBP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PliaFX Flo?

PliaFX Flo is a medical device that received FDA 510(k) clearance on 2024-11-21. The listed applicant is Lifenet Health. The 510(k) number is K242799.

When did PliaFX Flo receive FDA 510(k) clearance?

PliaFX Flo received FDA 510(k) clearance on 2024-11-21, under 510(k) number K242799.

Who is the listed applicant for PliaFX Flo?

The FDA 510(k) record lists Lifenet Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PliaFX Flo?

The FDA product code for PliaFX Flo is MBP.

Other records listing Lifenet Health 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.

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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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