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INFINION ENHANCEMENT PACKAGE

K011296 Class II Traditional
Decision Date
2001-07-19
Sponsor / Applicant
Philips Medical Systems (Cleveland), Inc.

Technical Specification

510(k) Submission ID K011296
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2001-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INFINION ENHANCEMENT PACKAGE received FDA 510(k) clearance under submission number K011296, 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 2001-07-19.

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.