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Access anti-HBc Total

K253687 Class II Traditional
Decision Date
2026-02-19
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K253687
Product Code SEI
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3173
Decision Date 2026-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Access anti-HBc Total received FDA 510(k) clearance under submission number K253687, sponsored by Beckman Coulter, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2026-02-19.

Classification & Regulation

This clearance is catalogued under FDA product code SEI and 21 CFR 866.3173, within the Microbiology review panel as a Class II device.