Documento fuente o registro público

FDA 510(k) K201258 — EASYMAX Tag Self-Monitoring Blood Glucose System

FDA 510(k) index record K201258. Device: EASYMAX Tag Self-Monitoring Blood Glucose System. Applicant as listed: Eps Bio Technology Corp.. Decision date: 2021-09-01.

OtherU.S. Food and Drug Administration (FDA)2021-09-01

Fuente

"device_name": "EASYMAX Tag Self-Monitoring Blood Glucose System"

Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.

Review and references

Reviewer

Automated FDA record verification

Published

2026-10-20

Updated

2026-10-31

Disclaimer

professional use

FDA 510(k) public index record K201258.

Device name: EASYMAX Tag Self-Monitoring Blood Glucose System. Applicant as listed: Eps Bio Technology Corp..

Decision date: 2021-09-01. Decision wording: Substantially Equivalent.

Product code: NBW. Regulation: 21 CFR 862.1345. Medical specialty: Clinical Chemistry.

This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.

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