meddevicedb.com FDA Device Reference

BIAD NUCLEAR IMAGING SYSTEM

K892875 Class II Traditional
Decision Date
1989-07-20
Sponsor / Applicant
Trionix Research Laboratory, Inc.

Technical Specification

510(k) Submission ID K892875
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 1989-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIAD NUCLEAR IMAGING SYSTEM received FDA 510(k) clearance under submission number K892875, sponsored by Trionix Research Laboratory, 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 1989-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.