FDA 510(k)

POSEIDON ST

K-Number: K261031 · 2026-07-10

Decision Date2026-07-10

Product CodeMQP

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

POSEIDON ST is the device name listed in this FDA 510(k) record. The listed applicant is Signus Medinzintechnik GmbH. It received FDA 510(k) clearance on 2026-07-10 under 510(k) number K261031. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSEIDON ST?

POSEIDON ST is a medical device that received FDA 510(k) clearance on 2026-07-10. The listed applicant is Signus Medinzintechnik GmbH. The 510(k) number is K261031.

When did POSEIDON ST receive FDA 510(k) clearance?

POSEIDON ST received FDA 510(k) clearance on 2026-07-10, under 510(k) number K261031.

Who is the listed applicant for POSEIDON ST?

The FDA 510(k) record lists Signus Medinzintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POSEIDON ST?

The FDA product code for POSEIDON ST is MQP.

Related Devices (Code: MQP)

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.

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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.