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FDA 510(k)

ImmersiveTouch

K-Number: K210726 · 2021-09-29

ApplicantImmersivetouch, Inc.
Decision Date2021-09-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ImmersiveTouch is a medical device manufactured by Immersivetouch, Inc.. It received FDA 510(k) clearance on 2021-09-29 under approval number K210726. 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 ImmersiveTouch?

ImmersiveTouch is a medical device that received FDA 510(k) clearance on 2021-09-29. It is manufactured by Immersivetouch, Inc.. The 510(k) number is K210726.

When was ImmersiveTouch approved by the FDA?

ImmersiveTouch received FDA 510(k) clearance on 2021-09-29, under approval number K210726.

What company makes ImmersiveTouch?

ImmersiveTouch is manufactured by Immersivetouch, Inc..

What is the FDA product code for ImmersiveTouch?

The FDA product code for ImmersiveTouch is LLZ.

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Official Source

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