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FDA 510(k)

LacriPro Punctum Plug

K-Number: K161673 · 2016-11-18

ApplicantLacrimedics, Inc.
Decision Date2016-11-18
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

LacriPro Punctum Plug is a medical device manufactured by Lacrimedics, Inc.. It received FDA 510(k) clearance on 2016-11-18 under approval number K161673. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LacriPro Punctum Plug?

LacriPro Punctum Plug is a medical device that received FDA 510(k) clearance on 2016-11-18. It is manufactured by Lacrimedics, Inc.. The 510(k) number is K161673.

When was LacriPro Punctum Plug approved by the FDA?

LacriPro Punctum Plug received FDA 510(k) clearance on 2016-11-18, under approval number K161673.

What company makes LacriPro Punctum Plug?

LacriPro Punctum Plug is manufactured by Lacrimedics, Inc..

What is the FDA product code for LacriPro Punctum Plug?

The FDA product code for LacriPro Punctum 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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