Accipiolx
K-Number: K201310 · 2020-08-07
Device Summary
Frequently Asked Questions
What is the Accipiolx?
Accipiolx is a medical device that received FDA 510(k) clearance on 2020-08-07. The listed applicant is Maxq AL , Ltd.. The 510(k) number is K201310.
When did Accipiolx receive FDA 510(k) clearance?
Accipiolx received FDA 510(k) clearance on 2020-08-07, under 510(k) number K201310.
Who is the listed applicant for Accipiolx?
The FDA 510(k) record lists Maxq AL , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Accipiolx?
The FDA product code for Accipiolx is QAS.
Other records listing Maxq AL , 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: QAS)
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.