Disposable Safety Lancet
K-Number: K222408 · 2022-11-29
Decision Date2022-11-29
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Disposable Safety Lancet is a medical device manufactured by Beijing Ruicheng Medical Supplies Co., Ltd.. It received FDA 510(k) clearance on 2022-11-29 under approval number K222408. 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 Disposable Safety Lancet?
Disposable Safety Lancet is a medical device that received FDA 510(k) clearance on 2022-11-29. It is manufactured by Beijing Ruicheng Medical Supplies Co., Ltd.. The 510(k) number is K222408.
When was Disposable Safety Lancet approved by the FDA?
Disposable Safety Lancet received FDA 510(k) clearance on 2022-11-29, under approval number K222408.
What company makes Disposable Safety Lancet?
Disposable Safety Lancet is manufactured by Beijing Ruicheng Medical Supplies Co., Ltd..
What is the FDA product code for Disposable Safety Lancet?
The FDA product code for Disposable Safety Lancet is FMK.
Related Clinical Trials
Other Devices by Beijing Ruicheng Medical Supplies 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.