Ikshana
K-Number: K230249 · 2023-10-16
ApplicantImmersivetouch
Decision Date2023-10-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Ikshana is a medical device manufactured by Immersivetouch. It received FDA 510(k) clearance on 2023-10-16 under approval number K230249. 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 Ikshana?
Ikshana is a medical device that received FDA 510(k) clearance on 2023-10-16. It is manufactured by Immersivetouch. The 510(k) number is K230249.
When was Ikshana approved by the FDA?
Ikshana received FDA 510(k) clearance on 2023-10-16, under approval number K230249.
What company makes Ikshana?
Ikshana is manufactured by Immersivetouch.
What is the FDA product code for Ikshana?
The FDA product code for Ikshana is LLZ.
Other Devices by Immersivetouch
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.