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VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HAV TOTAL REAGENT PACK,CALIBRATOR,CONTROLS

K060678 Class II Traditional
Decision Date
2006-09-14
Sponsor / Applicant
Ortho-Clinical Diagnostics, Inc.

Technical Specification

510(k) Submission ID K060678
Product Code LOL
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3310
Decision Date 2006-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITROS IMMUNODIAGNOSTIC PRODUCTS ANTI-HAV TOTAL REAGENT PACK,CALIBRATOR,CONTROLS received FDA 510(k) clearance under submission number K060678, sponsored by Ortho-Clinical Diagnostics, 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 2006-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code LOL and 21 CFR 866.3310, within the Microbiology review panel as a Class II device.