FDA 510(k)

MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS

K-Number: K962738 · 1996-10-10

Decision Date1996-10-10

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1996-10-10 under 510(k) number K962738. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS?

MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS is a medical device that received FDA 510(k) clearance on 1996-10-10. The listed applicant is GE Medical Systems. The 510(k) number is K962738.

When did MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS receive FDA 510(k) clearance?

MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS received FDA 510(k) clearance on 1996-10-10, under 510(k) number K962738.

Who is the listed applicant for MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS?

The FDA 510(k) record lists GE Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS?

The FDA product code for MILLENNIUM MT AND MILLENNIUM MG NUCLEAR MEDICINE SYSTEMS is KPS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing GE Medical Systems as applicant

K253808AIR Recon DL K220848Venue Fit K220851Venue K173341Vivid E80, Vivid E90, Vivid E95 K103411IDEAL IQ SOFTWARE OPTION K073138CARDIQ EXPRESS VERSION 2.0

View all 170 devices →

Related Devices (Code: KPS)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.