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NOMOS MOTORIZED CRANE II

K013036 Class II Traditional
Decision Date
2001-12-07
Sponsor / Applicant
Nomos Corp.

Technical Specification

510(k) Submission ID K013036
Product Code JAI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5770
Decision Date 2001-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOMOS MOTORIZED CRANE II received FDA 510(k) clearance under submission number K013036, 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 2001-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code JAI and 21 CFR 892.5770, within the Radiology review panel as a Class II device.