510(k) K223781

Quantisal™ II Oral Fluid Collection Device by Immunalysis Corporation — Product Code PJD

K223781 is an FDA 510(k) premarket notification submitted by Immunalysis Corporation for the device "Quantisal™ II Oral Fluid Collection Device". The FDA issued a decision of Substantially Equivalent on July 28, 2023. The device falls under product code PJD (Oral Fluid Drugs Of Abuse And Alcohol Test Specimen Collection Device), a Class II device regulated under 21 CFR 862.1675. Immunalysis Corporation has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 28, 2023
Date Received
December 16, 2022
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Oral Fluid Drugs Of Abuse And Alcohol Test Specimen Collection Device
Device Class
Class II
Regulation Number
862.1675
Review Panel
CH
Submission Type

Intended for use in the collection, preservation, and transport of oral fluid specimens for drugs of abuse or alcohol testing.