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)

ANYSCAN-S SPECT IMAGING SYSTEM

K-Number: K131625 · 2013-10-03

ApplicantAbsolute Imaging Solutions
Decision Date2013-10-03
Product CodeKPS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANYSCAN-S SPECT IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Absolute Imaging Solutions. It received FDA 510(k) clearance on 2013-10-03 under 510(k) number K131625. 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 ANYSCAN-S SPECT IMAGING SYSTEM?

ANYSCAN-S SPECT IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2013-10-03. The listed applicant is Absolute Imaging Solutions. The 510(k) number is K131625.

When did ANYSCAN-S SPECT IMAGING SYSTEM receive FDA 510(k) clearance?

ANYSCAN-S SPECT IMAGING SYSTEM received FDA 510(k) clearance on 2013-10-03, under 510(k) number K131625.

Who is the listed applicant for ANYSCAN-S SPECT IMAGING SYSTEM?

The FDA 510(k) record lists Absolute Imaging Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANYSCAN-S SPECT IMAGING SYSTEM?

The FDA product code for ANYSCAN-S SPECT IMAGING 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

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.

↑