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Healgen Accurate Urine Drug Screen Dip Card; Healgen Accurate Home Urine Drug Test Dip Card

K253567 Class II Traditional
Decision Date
2025-12-23
Sponsor / Applicant
Healgen Scientific,, LLC

Technical Specification

510(k) Submission ID K253567
Product Code NGL
Medical Specialty / Panel Clinical Toxicology
Regulation Citation 21 CFR 862.3650
Decision Date 2025-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Healgen Accurate Urine Drug Screen Dip Card; Healgen Accurate Home Urine Drug Test Dip Card received FDA 510(k) clearance under submission number K253567, sponsored by Healgen Scientific,, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Toxicology review panel. The statutory decision date of record is 2025-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code NGL and 21 CFR 862.3650, within the Clinical Toxicology review panel as a Class II device.