Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Safety Lancet

K-Number: K242627 · 2024-10-30

Decision Date2024-10-30
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Safety Lancet is a medical device manufactured by Ningbo Medsun Medical Co., Ltd.. It received FDA 510(k) clearance on 2024-10-30 under approval number K242627. 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 Safety Lancet?

Safety Lancet is a medical device that received FDA 510(k) clearance on 2024-10-30. It is manufactured by Ningbo Medsun Medical Co., Ltd.. The 510(k) number is K242627.

When was Safety Lancet approved by the FDA?

Safety Lancet received FDA 510(k) clearance on 2024-10-30, under approval number K242627.

What company makes Safety Lancet?

Safety Lancet is manufactured by Ningbo Medsun Medical Co., Ltd..

What is the FDA product code for Safety Lancet?

The FDA product code for Safety Lancet is FMK.

Other Devices by Ningbo Medsun Medical Co., Ltd.

View all 7 devices →

Related Devices (Code: FMK)

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.