FDA 510(k)

Ikshana

K-Number: K230249 · 2023-10-16

Decision Date2023-10-16

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Ikshana is the device name listed in this FDA 510(k) record. The listed applicant is Immersivetouch. It received FDA 510(k) clearance on 2023-10-16 under 510(k) 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. The listed applicant is Immersivetouch. The 510(k) number is K230249.

When did Ikshana receive FDA 510(k) clearance?

Ikshana received FDA 510(k) clearance on 2023-10-16, under 510(k) number K230249.

Who is the listed applicant for Ikshana?

The FDA 510(k) record lists Immersivetouch as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ikshana?

The FDA product code for Ikshana is LLZ.

Other records listing Immersivetouch as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K210726ImmersiveTouch K181813ImmersiveView Surgical Plan (IVSP®)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.