Cleared Traditional

K061398 - SNUG PLUG PUNCTUM PLUG

K061398 · Fci Ophthalmics, Inc. · Ophthalmic device
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Jul 2006
Decision
53d
Days
-
Risk

K061398 is an FDA 510(k) clearance for the SNUG PLUG PUNCTUM PLUG. Classified as Plug, Punctum (product code LZU).

Submitted by Fci Ophthalmics, Inc. (Centercille, US). The FDA issued a Cleared decision on July 11, 2006 after a review of 53 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Fci Ophthalmics, Inc. devices

FDA 510(k) Submission Details - K061398

510(k) Number K061398 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 19, 2006
Decision Date July 11, 2006
Days to Decision 53 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
57d faster than avg
Panel avg: 110d · This submission: 53d
Pathway characteristics
Predicate-based equivalence.

LZU Device Classification - Class 0,

Product Code LZU Plug, Punctum
Device Class -

Regulatory Peers - LZU Plug, Punctum

All 18
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