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FDA 510(k)

WACKERS-LIU CQ SOFTWARE

K-Number: K002229 · 2000-10-20

ApplicantEclipse Systems, Inc.
Decision Date2000-10-20
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WACKERS-LIU CQ SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Eclipse Systems, Inc.. It received FDA 510(k) clearance on 2000-10-20 under 510(k) number K002229. 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 WACKERS-LIU CQ SOFTWARE?

WACKERS-LIU CQ SOFTWARE is a medical device that received FDA 510(k) clearance on 2000-10-20. The listed applicant is Eclipse Systems, Inc.. The 510(k) number is K002229.

When did WACKERS-LIU CQ SOFTWARE receive FDA 510(k) clearance?

WACKERS-LIU CQ SOFTWARE received FDA 510(k) clearance on 2000-10-20, under 510(k) number K002229.

Who is the listed applicant for WACKERS-LIU CQ SOFTWARE?

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

What is the FDA product code for WACKERS-LIU CQ SOFTWARE?

The FDA product code for WACKERS-LIU CQ SOFTWARE 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 Eclipse Systems, Inc. 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.

K032500MODIFICARION TO WACKERS-LIU CQ SOFTWARE

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

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