LFR-260
K-Number: K233295 · 2024-05-31
ApplicantEvolution Optiks Limited
Decision Date2024-05-31
Product CodeSBI
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
LFR-260 is the device name listed in this FDA 510(k) record. The listed applicant is Evolution Optiks Limited. It received FDA 510(k) clearance on 2024-05-31 under 510(k) number K233295. The device is classified under product code SBI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LFR-260?
LFR-260 is a medical device that received FDA 510(k) clearance on 2024-05-31. The listed applicant is Evolution Optiks Limited. The 510(k) number is K233295.
When did LFR-260 receive FDA 510(k) clearance?
LFR-260 received FDA 510(k) clearance on 2024-05-31, under 510(k) number K233295.
Who is the listed applicant for LFR-260?
The FDA 510(k) record lists Evolution Optiks Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LFR-260?
The FDA product code for LFR-260 is SBI.
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.