FDA 510(k)

MuscleView

K-Number: K241331 · 2024-10-01

Decision Date2024-10-01

Product CodeLNH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MuscleView is the device name listed in this FDA 510(k) record. The listed applicant is Springbok, Inc.. It received FDA 510(k) clearance on 2024-10-01 under 510(k) number K241331. 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 MuscleView?

MuscleView is a medical device that received FDA 510(k) clearance on 2024-10-01. The listed applicant is Springbok, Inc.. The 510(k) number is K241331.

When did MuscleView receive FDA 510(k) clearance?

MuscleView received FDA 510(k) clearance on 2024-10-01, under 510(k) number K241331.

Who is the listed applicant for MuscleView?

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

What is the FDA product code for MuscleView?

The FDA product code for MuscleView is LNH.

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 Systems K261331I-Genius (100019400)Esaote, S.p.A.K260852MAGNETOM Flow.Elite;MAGNETOM Flow.Neo;MAGNETOM Flow.Rise;MAGNETOM Flow.PureSiemens Healthineers AG K260113uMR AstraShanghai United Imaging Healthcare Co., Ltd.K253862APERTO Lucent MRI SystemFujifilm Corporation K260746S-scan Open (100001800)Esaote, S.p.A.

Official Source

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