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XCT 2000 L PQCT BONE DENSITOMETER

K983273 Class II Traditional
Decision Date
1998-10-29
Sponsor / Applicant
Medical Systems, Inc.

Technical Specification

510(k) Submission ID K983273
Product Code KGI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1170
Decision Date 1998-10-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XCT 2000 L PQCT BONE DENSITOMETER received FDA 510(k) clearance under submission number K983273, sponsored by Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1998-10-29.

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.