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FDA 510(k)

DEEPECHO

K-Number: K242594 · 2025-05-23

ApplicantDeepecho
Decision Date2025-05-23
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DEEPECHO is a medical device manufactured by Deepecho. It received FDA 510(k) clearance on 2025-05-23 under approval number K242594. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEEPECHO?

DEEPECHO is a medical device that received FDA 510(k) clearance on 2025-05-23. It is manufactured by Deepecho. The 510(k) number is K242594.

When was DEEPECHO approved by the FDA?

DEEPECHO received FDA 510(k) clearance on 2025-05-23, under approval number K242594.

What company makes DEEPECHO?

DEEPECHO is manufactured by Deepecho.

What is the FDA product code for DEEPECHO?

The FDA product code for DEEPECHO is IYN.

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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.

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