meddevicedb.com FDA Device Reference

COMPUR M-1000 MINI-PHOTOMETER

K800059 Class II Traditional
Decision Date
1980-04-04
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K800059
Product Code KHG
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7500
Decision Date 1980-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPUR M-1000 MINI-PHOTOMETER received FDA 510(k) clearance under submission number K800059, sponsored by Miles Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1980-04-04.

Classification & Regulation

This clearance is catalogued under FDA product code KHG and 21 CFR 864.7500, within the Hematology review panel as a Class II device.