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CLINISTAT TDA SERIES

K823112 Class I Traditional
Decision Date
1982-11-29
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K823112
Product Code KHO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2560
Decision Date 1982-11-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLINISTAT TDA SERIES received FDA 510(k) clearance under submission number K823112, sponsored by Miles Laboratories, 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 1982-11-29.

Classification & Regulation

This clearance is catalogued under FDA product code KHO and 21 CFR 862.2560, within the Clinical Chemistry review panel as a Class I device.