SMR Reverse Liner
K-Number: K220792 · 2022-05-19
ApplicantLima Corporate S.P.A.
Decision Date2022-05-19
Product CodeMBF
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
SMR Reverse Liner is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2022-05-19 under approval number K220792. The device is classified under product code MBF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SMR Reverse Liner?
SMR Reverse Liner is a medical device that received FDA 510(k) clearance on 2022-05-19. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K220792.
When was SMR Reverse Liner approved by the FDA?
SMR Reverse Liner received FDA 510(k) clearance on 2022-05-19, under approval number K220792.
What company makes SMR Reverse Liner?
SMR Reverse Liner is manufactured by Lima Corporate S.P.A..
What is the FDA product code for SMR Reverse Liner?
The FDA product code for SMR Reverse Liner is MBF.
Other Devices by Lima Corporate S.P.A.
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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.