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MICROLAB M-MICROPROCESSOR DILUTER/DISP

K801913 Class I Traditional
Decision Date
1980-09-26
Sponsor / Applicant
Hamilton Co.

Technical Specification

510(k) Submission ID K801913
Product Code JQW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2750
Decision Date 1980-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROLAB M-MICROPROCESSOR DILUTER/DISP received FDA 510(k) clearance under submission number K801913, sponsored by Hamilton Co.. 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 1980-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code JQW and 21 CFR 862.2750, within the Clinical Chemistry review panel as a Class I device.