Libby Echo:Prio
K-Number: K220956 · 2022-07-20
Device Summary
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. The listed applicant is Dyad Medical, Inc.. The 510(k) number is K220956.
When did Libby Echo:Prio receive FDA 510(k) clearance?
Libby Echo:Prio received FDA 510(k) clearance on 2022-07-20, under 510(k) number K220956.
Who is the listed applicant for Libby Echo:Prio?
The FDA 510(k) record lists Dyad Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Libby Echo:Prio?
The FDA product code for Libby Echo:Prio is QIH.
Other records listing Dyad Medical, Inc. 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.
Related Devices (Code: QIH)
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.
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.