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WISCONSIN BONE MINERAL ANALYZER

K802181 Class II Traditional
Decision Date
1980-12-31
Sponsor / Applicant
Lunar Radiation Corp.

Technical Specification

510(k) Submission ID K802181
Product Code KGI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1170
Decision Date 1980-12-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WISCONSIN BONE MINERAL ANALYZER received FDA 510(k) clearance under submission number K802181, 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 1980-12-31.

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.