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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Medsun Medical Co., Ltd.. It received FDA 510(k) clearance on 2024-01-04 under 510(k) 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. The listed applicant is Ningbo Medsun Medical Co., Ltd.. The 510(k) number is K232330.

When did Lancing System receive FDA 510(k) clearance?

Lancing System received FDA 510(k) clearance on 2024-01-04, under 510(k) number K232330.

Who is the listed applicant for Lancing System?

The FDA 510(k) record lists Ningbo Medsun Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Lancing System?

The FDA product code for Lancing System is QRK.

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Related Devices (Code: QRK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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