SonoMSK
K-Number: K243690 · 2025-07-01
ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2025-07-01
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
SonoMSK is a medical device manufactured by PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2025-07-01 under approval number K243690. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SonoMSK?
SonoMSK is a medical device that received FDA 510(k) clearance on 2025-07-01. It is manufactured by PAJUNK GmbH Medizintechnologie. The 510(k) number is K243690.
When was SonoMSK approved by the FDA?
SonoMSK received FDA 510(k) clearance on 2025-07-01, under approval number K243690.
What company makes SonoMSK?
SonoMSK is manufactured by PAJUNK GmbH Medizintechnologie.
What is the FDA product code for SonoMSK?
The FDA product code for SonoMSK is BSP.
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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.