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

FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Beijing Ruicheng Medical Supplies Co., Ltd.. It received FDA 510(k) clearance on 2022-11-29 under 510(k) 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. The listed applicant is Beijing Ruicheng Medical Supplies Co., Ltd.. The 510(k) number is K222408.

When did Disposable Safety Lancet receive FDA 510(k) clearance?

Disposable Safety Lancet received FDA 510(k) clearance on 2022-11-29, under 510(k) number K222408.

Who is the listed applicant for Disposable Safety Lancet?

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

What is the FDA product code for Disposable Safety Lancet?

The FDA product code for Disposable Safety Lancet is FMK.

Other records listing Beijing Ruicheng Medical Supplies Co., Ltd. as applicant

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.

Related Devices (Code: FMK)

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.

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.