Accipiolx
K-Number: K182177 · 2018-10-26
ApplicantMaxq-Al , Ltd.
Decision Date2018-10-26
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 2018-10-26 under approval number K182177. 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 2018-10-26. It is manufactured by Maxq-Al , Ltd.. The 510(k) number is K182177.
When was Accipiolx approved by the FDA?
Accipiolx received FDA 510(k) clearance on 2018-10-26, under approval number K182177.
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.