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MRGP OPTICAL TRACKING UNIT

K991943 Class II Traditional
Decision Date
1999-08-23
Sponsor / Applicant
Philips Medical Systems (Cleveland), Inc.

Technical Specification

510(k) Submission ID K991943
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 1999-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MRGP OPTICAL TRACKING UNIT received FDA 510(k) clearance under submission number K991943, sponsored by Philips Medical Systems (Cleveland), 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 1999-08-23.

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.