meddevicedb.com FDA Device Reference

OEC 902, 901 NASA II, OEC 902, 901 NASA I CCD C-ARM

K955251 Class II Traditional
Decision Date
1996-04-12
Sponsor / Applicant
Imaging Services, Inc.

Technical Specification

510(k) Submission ID K955251
Product Code OXO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 1996-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OEC 902, 901 NASA II, OEC 902, 901 NASA I CCD C-ARM received FDA 510(k) clearance under submission number K955251, sponsored by Imaging Services, 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 1996-04-12.

Classification & Regulation

This clearance is catalogued under FDA product code OXO and 21 CFR 892.1650, within the Radiology review panel as a Class II device.