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Quantisal Oral Fluid Collection Device

K200801 Class II Traditional
Decision Date
2020-07-28
Sponsor / Applicant
Immunalysis Corporation

Technical Specification

510(k) Submission ID K200801
Product Code PJD
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 2020-07-28
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 K200801, 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 2020-07-28.

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.