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IND ONE STEP HCG URINE PREGNANCY TEST (STRIP)

K110889 Class II Traditional
Decision Date
2011-06-20
Sponsor / Applicant
Ind Diagnostics, Inc.

Technical Specification

510(k) Submission ID K110889
Product Code LCX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 2011-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IND ONE STEP HCG URINE PREGNANCY TEST (STRIP) received FDA 510(k) clearance under submission number K110889, sponsored by Ind Diagnostics, 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 2011-06-20.

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.