meddevicedb.com FDA Device Reference

AUTOMATIC BIOCHEMICAL ANALYZER

K810063 Class I Traditional
Decision Date
1981-01-26
Sponsor / Applicant
Acculab

Technical Specification

510(k) Submission ID K810063
Product Code JQP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2100
Decision Date 1981-01-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTOMATIC BIOCHEMICAL ANALYZER received FDA 510(k) clearance under submission number K810063, sponsored by Acculab. 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 1981-01-26.

Classification & Regulation

This clearance is catalogued under FDA product code JQP and 21 CFR 862.2100, within the Clinical Chemistry review panel as a Class I device.