meddevicedb.com FDA Device Reference

Simplexa Flu A/B & RSV Direct and Simplexa Flu A/B & RSV Positive Control Pack

K152408 Class II Special
Decision Date
2015-09-21
Sponsor / Applicant
Focus Diagnostics, Inc.

Technical Specification

510(k) Submission ID K152408
Product Code OCC
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3980
Decision Date 2015-09-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Simplexa Flu A/B & RSV Direct and Simplexa Flu A/B & RSV Positive Control Pack received FDA 510(k) clearance under submission number K152408, sponsored by Focus Diagnostics, 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 2015-09-21.

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.