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AP 72OS SEMI-AUTOMATED INSTRUMENT

K112910 Class II Traditional
Decision Date
2012-12-20
Sponsor / Applicant
Hitachi Chemical Diagnostics, Inc.

Technical Specification

510(k) Submission ID K112910
Product Code DHB
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5750
Decision Date 2012-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AP 72OS SEMI-AUTOMATED INSTRUMENT received FDA 510(k) clearance under submission number K112910, sponsored by Hitachi Chemical Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2012-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code DHB and 21 CFR 866.5750, within the Immunology review panel as a Class II device.