FDA 510(k)

medilogFD

K-Number: K253562 · 2026-08-14

Decision Date2026-08-14

Product CodeMWJ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

medilogFD is the device name listed in this FDA 510(k) record. The listed applicant is Schiller AG. It received FDA 510(k) clearance on 2026-08-14 under 510(k) number K253562. The device is classified under product code MWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the medilogFD?

medilogFD is a medical device that received FDA 510(k) clearance on 2026-08-14. The listed applicant is Schiller AG. The 510(k) number is K253562.

When did medilogFD receive FDA 510(k) clearance?

medilogFD received FDA 510(k) clearance on 2026-08-14, under 510(k) number K253562.

Who is the listed applicant for medilogFD?

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

What is the FDA product code for medilogFD?

The FDA product code for medilogFD is MWJ.

Other records listing Schiller AG 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.

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Related Devices (Code: MWJ)

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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.