Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GE QUASAR NUCLEAR MEDICINE SYSTEM

K-Number: K022960 · 2002-09-19

ApplicantGe Medical Systems F.I. Haifa
Decision Date2002-09-19
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE QUASAR NUCLEAR MEDICINE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems F.I. Haifa. It received FDA 510(k) clearance on 2002-09-19 under 510(k) number K022960. 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 GE QUASAR NUCLEAR MEDICINE SYSTEM?

GE QUASAR NUCLEAR MEDICINE SYSTEM is a medical device that received FDA 510(k) clearance on 2002-09-19. The listed applicant is Ge Medical Systems F.I. Haifa. The 510(k) number is K022960.

When did GE QUASAR NUCLEAR MEDICINE SYSTEM receive FDA 510(k) clearance?

GE QUASAR NUCLEAR MEDICINE SYSTEM received FDA 510(k) clearance on 2002-09-19, under 510(k) number K022960.

Who is the listed applicant for GE QUASAR NUCLEAR MEDICINE SYSTEM?

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

What is the FDA product code for GE QUASAR NUCLEAR MEDICINE SYSTEM?

The FDA product code for GE QUASAR NUCLEAR MEDICINE SYSTEM 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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ge Medical Systems F.I. Haifa as applicant

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.

K130884XELERIS 3.1 PROCESSING AND REVIEW WORKSTATIONK093982XELERIS 3 PROCESSING AND REVIEW WORKSTATIONK093514DISCOVERY MODEL NM/CT 670K083504GE DISCOVERY NM/CT 570CK080124VENTRI 1.1K051855VENTRI

View all 17 devices →

Related Devices (Code: KPS)

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.

K261305MICSI-PETMicrostructure Imaging, Inc.K261427uMI Panvivo (uMI Panvivo M)Shanghai United Imaging Healthcare Co., Ltd.K261315Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 FamilySiemens Medical Solutions USA, Inc.K260524uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K253564uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)Shanghai United Imaging Healthcare Co., Ltd.K254001VERITON CT 300 Series Digital SPECT/CT System (VERITON CT 316/364); VERITON CT 400 Series Digital SPECT/CT System (VERITON CT 416/464)Spectrum Dynamics Medical, Ltd.

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.

↑