Accipiolx
K-Number: K201310 · 2020-08-07
ApplicantMaxq AL , Ltd.
Decision Date2020-08-07
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Accipiolx is a medical device manufactured by Maxq AL , Ltd.. It received FDA 510(k) clearance on 2020-08-07 under approval number K201310. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Accipiolx?
Accipiolx is a medical device that received FDA 510(k) clearance on 2020-08-07. It is manufactured by Maxq AL , Ltd.. The 510(k) number is K201310.
When was Accipiolx approved by the FDA?
Accipiolx received FDA 510(k) clearance on 2020-08-07, under approval number K201310.
What company makes Accipiolx?
Accipiolx is manufactured by Maxq AL , Ltd..
What is the FDA product code for Accipiolx?
The FDA product code for Accipiolx is QAS.
Related Devices (Code: QAS)
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.