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LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913

K093498 Class I Traditional
Decision Date
2009-12-14
Sponsor / Applicant
DiaSorin, Inc.

Technical Specification

510(k) Submission ID K093498
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2009-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIAISON N-TACT PTH CALIBRATION VERIFIERS MODEL 310913 received FDA 510(k) clearance under submission number K093498, sponsored by DiaSorin, 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 2009-12-14.

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.