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FDA 510(k)

Visant Medical Canalicular Plug

K-Number: K222164 · 2022-12-23

ApplicantVisant Medical, Inc.
Decision Date2022-12-23
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

Visant Medical Canalicular Plug is a medical device manufactured by Visant Medical, Inc.. It received FDA 510(k) clearance on 2022-12-23 under approval number K222164. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Visant Medical Canalicular Plug?

Visant Medical Canalicular Plug is a medical device that received FDA 510(k) clearance on 2022-12-23. It is manufactured by Visant Medical, Inc.. The 510(k) number is K222164.

When was Visant Medical Canalicular Plug approved by the FDA?

Visant Medical Canalicular Plug received FDA 510(k) clearance on 2022-12-23, under approval number K222164.

What company makes Visant Medical Canalicular Plug?

Visant Medical Canalicular Plug is manufactured by Visant Medical, Inc..

What is the FDA product code for Visant Medical Canalicular Plug?

The FDA product code for Visant Medical Canalicular Plug is LZU.

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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.

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