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BONE MINERAL ANALYZER CONTROLLER

K810159 Class II Traditional
Decision Date
1981-02-12
Sponsor / Applicant
Lunar Radiation Corp.

Technical Specification

510(k) Submission ID K810159
Product Code KGI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1170
Decision Date 1981-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BONE MINERAL ANALYZER CONTROLLER received FDA 510(k) clearance under submission number K810159, sponsored by Lunar Radiation Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1981-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code KGI and 21 CFR 892.1170, within the Radiology review panel as a Class II device.