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One Step hCG Pregnancy Test

K150063 Class II Traditional
Decision Date
2015-10-02
Sponsor / Applicant
Coretests, Inc.

Technical Specification

510(k) Submission ID K150063
Product Code LCX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 2015-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

One Step hCG Pregnancy Test received FDA 510(k) clearance under submission number K150063, sponsored by Coretests, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2015-10-02.

Classification & Regulation

This clearance is catalogued under FDA product code LCX and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.