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)

VitruvianScan (v1.0)

K-Number: K241925 · 2024-10-02

ApplicantPerspectum, Ltd.
Decision Date2024-10-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VitruvianScan (v1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Perspectum, Ltd.. It received FDA 510(k) clearance on 2024-10-02 under 510(k) number K241925. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VitruvianScan (v1.0)?

VitruvianScan (v1.0) is a medical device that received FDA 510(k) clearance on 2024-10-02. The listed applicant is Perspectum, Ltd.. The 510(k) number is K241925.

When did VitruvianScan (v1.0) receive FDA 510(k) clearance?

VitruvianScan (v1.0) received FDA 510(k) clearance on 2024-10-02, under 510(k) number K241925.

Who is the listed applicant for VitruvianScan (v1.0)?

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

What is the FDA product code for VitruvianScan (v1.0)?

The FDA product code for VitruvianScan (v1.0) is LNH.

Other records listing Perspectum, Ltd. 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.

K253413LiverMultiScan (v6.0)K233930MRCP+ version 2 (MRCP+ v2)K230294CoverScan (CoverScan v1.1)K213960LiverMultiScan v5 (LMSv5)K212565CoverScan v1K203280Hepatica v1 (Hepatica v1.0.0)

View all 8 devices →

Related Devices (Code: LNH)

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.

K253808AIR Recon DLGE Medical SystemsK261331I-Genius (100019400)Esaote, S.p.A.K260852MAGNETOM Flow.Elite;MAGNETOM Flow.Neo;MAGNETOM Flow.Rise;MAGNETOM Flow.PureSiemens Healthineers AGK260113uMR AstraShanghai United Imaging Healthcare Co., Ltd.K253862APERTO Lucent MRI SystemFujifilm CorporationK260746S-scan Open (100001800)Esaote, S.p.A.

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.

↑