JiveX
K-Number: K162008 · 2016-09-16
ApplicantVisus Technology Transfer GmbH
Decision Date2016-09-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
JiveX is a medical device manufactured by Visus Technology Transfer GmbH. It received FDA 510(k) clearance on 2016-09-16 under approval number K162008. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the JiveX?
JiveX is a medical device that received FDA 510(k) clearance on 2016-09-16. It is manufactured by Visus Technology Transfer GmbH. The 510(k) number is K162008.
When was JiveX approved by the FDA?
JiveX received FDA 510(k) clearance on 2016-09-16, under approval number K162008.
What company makes JiveX?
JiveX is manufactured by Visus Technology Transfer GmbH.
What is the FDA product code for JiveX?
The FDA product code for JiveX is LLZ.
Related Devices (Code: LLZ)
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.