meddevicedb.com FDA Device Reference

ID NOW Influenza A & B 2

K232775 Class II Special
Decision Date
2023-10-10
Sponsor / Applicant
Abbott Diagnostics Scarborough, Inc.

Technical Specification

510(k) Submission ID K232775
Product Code OCC
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3980
Decision Date 2023-10-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ID NOW Influenza A & B 2 received FDA 510(k) clearance under submission number K232775, sponsored by Abbott Diagnostics Scarborough, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2023-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code OCC and 21 CFR 866.3980, within the Microbiology review panel as a Class II device.