Lancing System
K-Number: K232330 · 2024-01-04
ApplicantNingbo Medsun Medical Co., Ltd.
Decision Date2024-01-04
Product CodeQRK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Lancing System is a medical device manufactured by Ningbo Medsun Medical Co., Ltd.. It received FDA 510(k) clearance on 2024-01-04 under approval number K232330. The device is classified under product code QRK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Lancing System?
Lancing System is a medical device that received FDA 510(k) clearance on 2024-01-04. It is manufactured by Ningbo Medsun Medical Co., Ltd.. The 510(k) number is K232330.
When was Lancing System approved by the FDA?
Lancing System received FDA 510(k) clearance on 2024-01-04, under approval number K232330.
What company makes Lancing System?
Lancing System is manufactured by Ningbo Medsun Medical Co., Ltd..
What is the FDA product code for Lancing System?
The FDA product code for Lancing System is QRK.
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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.