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)

RAYSCAN a-Expert

K-Number: K232325 · 2024-04-18

ApplicantRay Co., Ltd.
Decision Date2024-04-18
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RAYSCAN a-Expert is a medical device manufactured by Ray Co., Ltd.. It received FDA 510(k) clearance on 2024-04-18 under approval number K232325. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAYSCAN a-Expert?

RAYSCAN a-Expert is a medical device that received FDA 510(k) clearance on 2024-04-18. It is manufactured by Ray Co., Ltd.. The 510(k) number is K232325.

When was RAYSCAN a-Expert approved by the FDA?

RAYSCAN a-Expert received FDA 510(k) clearance on 2024-04-18, under approval number K232325.

What company makes RAYSCAN a-Expert?

RAYSCAN a-Expert is manufactured by Ray Co., Ltd..

What is the FDA product code for RAYSCAN a-Expert?

The FDA product code for RAYSCAN a-Expert is MUH.

Other Devices by Ray Co., Ltd.

View all 17 devices →

Related Devices (Code: MUH)

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.