Myriad Particles
K-Number: K200502 · 2021-03-31
Device Summary
Frequently Asked Questions
What is the Myriad Particles?
Myriad Particles is a medical device that received FDA 510(k) clearance on 2021-03-31. The listed applicant is Aroa Biosurgery , Ltd.. The 510(k) number is K200502.
When did Myriad Particles receive FDA 510(k) clearance?
Myriad Particles received FDA 510(k) clearance on 2021-03-31, under 510(k) number K200502.
Who is the listed applicant for Myriad Particles?
The FDA 510(k) record lists Aroa Biosurgery , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Myriad Particles?
The FDA product code for Myriad Particles is KGN.
Related Clinical Trials
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.
Other records listing Aroa Biosurgery , Ltd. 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: KGN)
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.