FDA 510(k) clearance · back to tracker

ULTIMUS Series Ultrasound Diagnostic System

Vinno Technology (Suzhou) Co.,Ltd cleared K240676 on 2024-12-16, decision: substantially equivalent

K-number

K240676

Sponsor

Vinno Technology (Suzhou) Co.,Ltd

Device

ULTIMUS Series Ultrasound Diagnostic System

Class

Class II

Decision

Substantially Equivalent

Decision date

2024-12-16

Product code

IYN

Advisory committee

Radiology

Medical specialty

Radiology

Regulation number

892.1550

Official FDA record

Open K240676on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

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Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.