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VITROS IMMUNODIAGNOSTIC PRODUCTS HBSAG CONTROLS

K011250 Class I Traditional
Decision Date
2001-06-13
Sponsor / Applicant
Ortho-Clinical Diagnostics, Inc.

Technical Specification

510(k) Submission ID K011250
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2001-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITROS IMMUNODIAGNOSTIC PRODUCTS HBSAG CONTROLS received FDA 510(k) clearance under submission number K011250, sponsored by Ortho-Clinical Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2001-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code JJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.