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TOUCHPACS SUITE

K112008 Class II Traditional
Decision Date
2012-01-06
Sponsor / Applicant
Touch Medical Solutions, Inc.

Technical Specification

510(k) Submission ID K112008
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2012-01-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOUCHPACS SUITE received FDA 510(k) clearance under submission number K112008, sponsored by Touch Medical Solutions, 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 2012-01-06.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.