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Quantisal™ Oral Fluid Collection Device

K232898 Class II Traditional
Decision Date
2023-11-21
Sponsor / Applicant
Immunalysis Corporation

Technical Specification

510(k) Submission ID K232898
Product Code PJD
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 2023-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Quantisal™ Oral Fluid Collection Device received FDA 510(k) clearance under submission number K232898, sponsored by Immunalysis Corporation. 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 2023-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code PJD and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.