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BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6

K070611 Class II Traditional
Decision Date
2007-07-11
Sponsor / Applicant
Nomos Corp.

Technical Specification

510(k) Submission ID K070611
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2007-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BAT ULTRASOUND LOCALIZATION AND POSITIONING SYSTEM, VERSION 6 received FDA 510(k) clearance under submission number K070611, sponsored by Nomos Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2007-07-11.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.