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H.I.STANDARD CALIBRE UPGRADE

K911746 Class II Traditional
Decision Date
1991-08-16
Sponsor / Applicant
Health Images, Inc.

Technical Specification

510(k) Submission ID K911746
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 1991-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

H.I.STANDARD CALIBRE UPGRADE received FDA 510(k) clearance under submission number K911746, sponsored by Health Images, 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 1991-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.