FDA 510(k) clearance · back to tracker

Surgical Power System

Guizhou Zirui Technology Co., Ltd. cleared K254174 on 2026-09-11, decision: substantially equivalent

K-number

K254174

Sponsor

Guizhou Zirui Technology Co., Ltd.

Device

Surgical Power System

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-09-11

Product code

HBC

Advisory committee

Neurology

Medical specialty

Neurology

Regulation number

882.4360

Official FDA record

Open K254174on accessdata.fda.gov →

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

openFDA JSON

Raw record →

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.