MedtFine Safety Lancet
K-Number: K241848 · 2024-08-20
Decision Date2024-08-20
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
MedtFine Safety Lancet is a medical device manufactured by Ningbo Caremed Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2024-08-20 under approval number K241848. 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 MedtFine Safety Lancet?
MedtFine Safety Lancet is a medical device that received FDA 510(k) clearance on 2024-08-20. It is manufactured by Ningbo Caremed Medical Products Co., Ltd.. The 510(k) number is K241848.
When was MedtFine Safety Lancet approved by the FDA?
MedtFine Safety Lancet received FDA 510(k) clearance on 2024-08-20, under approval number K241848.
What company makes MedtFine Safety Lancet?
MedtFine Safety Lancet is manufactured by Ningbo Caremed Medical Products Co., Ltd..
What is the FDA product code for MedtFine Safety Lancet?
The FDA product code for MedtFine Safety Lancet is FMK.
Other Devices by Ningbo Caremed Medical Products Co., Ltd.
Related Devices (Code: FMK)
K153670Genteel Lancing DeviceGenteel, LLC
K172712gentleheel Micro-Preemie, gentleheel Preemie, gentleheel Newborn, gentleheel ToddlerGri Medical & Electronic Technology Co., Ltd.
K193009Promisemed Heel Blood LancetPromisemed Hangzhou Meditech Co., Ltd.
K192666Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety LancetPromisemed Hangzhou Meditech Co., Ltd.
K210745Heel Incision Safety LancetSteriLance Medical (Suzhou), Inc.
K223243BD Microtainer® Contact-Activated Lancets; BD Microtainer® Quikheel LancetsBecton, Dickinson and Company
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.