JBS-LVO
K-Number: K241480 · 2024-09-27
ApplicantJLK, Inc.
Decision Date2024-09-27
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
JBS-LVO is a medical device manufactured by JLK, Inc.. It received FDA 510(k) clearance on 2024-09-27 under approval number K241480. 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 JBS-LVO?
JBS-LVO is a medical device that received FDA 510(k) clearance on 2024-09-27. It is manufactured by JLK, Inc.. The 510(k) number is K241480.
When was JBS-LVO approved by the FDA?
JBS-LVO received FDA 510(k) clearance on 2024-09-27, under approval number K241480.
What company makes JBS-LVO?
JBS-LVO is manufactured by JLK, Inc..
What is the FDA product code for JBS-LVO?
The FDA product code for JBS-LVO is QAS.
Other Devices by JLK, Inc.
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.