SurgiLance® Safety Lancet
K-Number: K222224 · 2022-09-22
ApplicantMedipurpose Pte. , Ltd.
Decision Date2022-09-22
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
SurgiLance® Safety Lancet is a medical device manufactured by Medipurpose Pte. , Ltd.. It received FDA 510(k) clearance on 2022-09-22 under approval number K222224. 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 SurgiLance® Safety Lancet?
SurgiLance® Safety Lancet is a medical device that received FDA 510(k) clearance on 2022-09-22. It is manufactured by Medipurpose Pte. , Ltd.. The 510(k) number is K222224.
When was SurgiLance® Safety Lancet approved by the FDA?
SurgiLance® Safety Lancet received FDA 510(k) clearance on 2022-09-22, under approval number K222224.
What company makes SurgiLance® Safety Lancet?
SurgiLance® Safety Lancet is manufactured by Medipurpose Pte. , Ltd..
What is the FDA product code for SurgiLance® Safety Lancet?
The FDA product code for SurgiLance® Safety Lancet 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.