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FDA 510(k)

SNUG PLUG PUNCTUM PLUG

K-Number: K061398 · 2006-07-11

ApplicantFci Ophthalmics, Inc.
Decision Date2006-07-11
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

SNUG PLUG PUNCTUM PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Fci Ophthalmics, Inc.. It received FDA 510(k) clearance on 2006-07-11 under 510(k) number K061398. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNUG PLUG PUNCTUM PLUG?

SNUG PLUG PUNCTUM PLUG is a medical device that received FDA 510(k) clearance on 2006-07-11. The listed applicant is Fci Ophthalmics, Inc.. The 510(k) number is K061398.

When did SNUG PLUG PUNCTUM PLUG receive FDA 510(k) clearance?

SNUG PLUG PUNCTUM PLUG received FDA 510(k) clearance on 2006-07-11, under 510(k) number K061398.

Who is the listed applicant for SNUG PLUG PUNCTUM PLUG?

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

What is the FDA product code for SNUG PLUG PUNCTUM PLUG?

The FDA product code for SNUG PLUG 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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