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 a medical device manufactured by Lifenet Health. It received FDA 510(k) clearance on 2024-11-21 under approval 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. It is manufactured by Lifenet Health. The 510(k) number is K242799.
When was PliaFX Flo approved by the FDA?
PliaFX Flo received FDA 510(k) clearance on 2024-11-21, under approval number K242799.
What company makes PliaFX Flo?
PliaFX Flo is manufactured by Lifenet Health.
What is the FDA product code for PliaFX Flo?
The FDA product code for PliaFX Flo is MBP.
Other Devices by Lifenet Health
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.