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FDA 510(k)

Libby Echo:Prio

K-Number: K220956 · 2022-07-20

ApplicantDyad Medical, Inc.
Decision Date2022-07-20
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Libby Echo:Prio is a medical device manufactured by Dyad Medical, Inc.. It received FDA 510(k) clearance on 2022-07-20 under approval number K220956. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Libby Echo:Prio?

Libby Echo:Prio is a medical device that received FDA 510(k) clearance on 2022-07-20. It is manufactured by Dyad Medical, Inc.. The 510(k) number is K220956.

When was Libby Echo:Prio approved by the FDA?

Libby Echo:Prio received FDA 510(k) clearance on 2022-07-20, under approval number K220956.

What company makes Libby Echo:Prio?

Libby Echo:Prio is manufactured by Dyad Medical, Inc..

What is the FDA product code for Libby Echo:Prio?

The FDA product code for Libby Echo:Prio is QIH.

Other Devices by Dyad Medical, Inc.

K210931Libby IAAA v1.0

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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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