Medifun Safety Lancet ( MSL1 series)
K-Number: K241750 · 2024-08-15
ApplicantMedifun Corporation
Decision Date2024-08-15
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Medifun Safety Lancet ( MSL1 series) is a medical device manufactured by Medifun Corporation. It received FDA 510(k) clearance on 2024-08-15 under approval number K241750. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Medifun Safety Lancet ( MSL1 series)?
Medifun Safety Lancet ( MSL1 series) is a medical device that received FDA 510(k) clearance on 2024-08-15. It is manufactured by Medifun Corporation. The 510(k) number is K241750.
When was Medifun Safety Lancet ( MSL1 series) approved by the FDA?
Medifun Safety Lancet ( MSL1 series) received FDA 510(k) clearance on 2024-08-15, under approval number K241750.
What company makes Medifun Safety Lancet ( MSL1 series)?
Medifun Safety Lancet ( MSL1 series) is manufactured by Medifun Corporation.
What is the FDA product code for Medifun Safety Lancet ( MSL1 series)?
The FDA product code for Medifun Safety Lancet ( MSL1 series) is FMK.
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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.