Disposable Sterile Lancet
K-Number: K222055 · 2022-11-15
Decision Date2022-11-15
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Disposable Sterile Lancet is a medical device manufactured by Tianjin Rilifine Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2022-11-15 under approval number K222055. 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 Sterile Lancet?
Disposable Sterile Lancet is a medical device that received FDA 510(k) clearance on 2022-11-15. It is manufactured by Tianjin Rilifine Medical Device Co., Ltd.. The 510(k) number is K222055.
When was Disposable Sterile Lancet approved by the FDA?
Disposable Sterile Lancet received FDA 510(k) clearance on 2022-11-15, under approval number K222055.
What company makes Disposable Sterile Lancet?
Disposable Sterile Lancet is manufactured by Tianjin Rilifine Medical Device Co., Ltd..
What is the FDA product code for Disposable Sterile Lancet?
The FDA product code for Disposable Sterile Lancet is FMK.
Other Devices by Tianjin Rilifine Medical Device Co., Ltd.
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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.