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ALT-QUANTICHROM

K812926 Class I Traditional
Decision Date
1981-11-06
Sponsor / Applicant
Abbott Laboratories

Technical Specification

510(k) Submission ID K812926
Product Code CKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1981-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALT-QUANTICHROM received FDA 510(k) clearance under submission number K812926, sponsored by Abbott Laboratories. 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 1981-11-06.

Classification & Regulation

This clearance is catalogued under FDA product code CKA and 21 CFR 862.1030, within the Clinical Chemistry review panel as a Class I device.