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CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5)

K252672 Class II Traditional
Decision Date
2026-02-20
Sponsor / Applicant
Casebioscience, Inc.

Technical Specification

510(k) Submission ID K252672
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2026-02-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5) received FDA 510(k) clearance under submission number K252672, sponsored by Casebioscience, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2026-02-20.

Classification & Regulation

This clearance is catalogued under FDA product code MQL and 21 CFR 884.6180, within the Obstetrics/Gynecology review panel as a Class II device.