VS-370CF, VS-370CT
K-Number: K262152 · 2026-07-24
Device Summary
Frequently Asked Questions
What is the VS-370CF, VS-370CT?
VS-370CF, VS-370CT is a medical device that received FDA 510(k) clearance on 2026-07-24. The listed applicant is VISION MEDICAL Co., Ltd.. The 510(k) number is K262152.
When did VS-370CF, VS-370CT receive FDA 510(k) clearance?
VS-370CF, VS-370CT received FDA 510(k) clearance on 2026-07-24, under 510(k) number K262152.
Who is the listed applicant for VS-370CF, VS-370CT?
The FDA 510(k) record lists VISION MEDICAL Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VS-370CF, VS-370CT?
The FDA product code for VS-370CF, VS-370CT is FCX.
Related Devices (Code: FCX)
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.