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FILMARRAY RP PANEL

K120267 Class II Traditional
Decision Date
2012-05-15
Sponsor / Applicant
Idaho Technology, Inc.

Technical Specification

510(k) Submission ID K120267
Product Code OCC
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3980
Decision Date 2012-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FILMARRAY RP PANEL received FDA 510(k) clearance under submission number K120267, sponsored by Idaho Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2012-05-15.

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.