Arkligners
K-Number: K220835 · 2022-08-12
ApplicantArklign Laboratories
Decision Date2022-08-12
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Arkligners is a medical device manufactured by Arklign Laboratories. It received FDA 510(k) clearance on 2022-08-12 under approval number K220835. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Arkligners?
Arkligners is a medical device that received FDA 510(k) clearance on 2022-08-12. It is manufactured by Arklign Laboratories. The 510(k) number is K220835.
When was Arkligners approved by the FDA?
Arkligners received FDA 510(k) clearance on 2022-08-12, under approval number K220835.
What company makes Arkligners?
Arkligners is manufactured by Arklign Laboratories.
What is the FDA product code for Arkligners?
The FDA product code for Arkligners is NXC.
Related Devices (Code: NXC)
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.