LimFlow V-Ceiver
K-Number: K242776 · 2025-02-14
ApplicantLimFlow, Inc.
Decision Date2025-02-14
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
LimFlow V-Ceiver is a medical device manufactured by LimFlow, Inc.. It received FDA 510(k) clearance on 2025-02-14 under approval number K242776. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LimFlow V-Ceiver?
LimFlow V-Ceiver is a medical device that received FDA 510(k) clearance on 2025-02-14. It is manufactured by LimFlow, Inc.. The 510(k) number is K242776.
When was LimFlow V-Ceiver approved by the FDA?
LimFlow V-Ceiver received FDA 510(k) clearance on 2025-02-14, under approval number K242776.
What company makes LimFlow V-Ceiver?
LimFlow V-Ceiver is manufactured by LimFlow, Inc..
What is the FDA product code for LimFlow V-Ceiver?
The FDA product code for LimFlow V-Ceiver is MMX.
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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.