Cleared Traditional

K946357 - COLLAGEN INTRACANALICULAR PLUG

K946357 · Oasis Medical, Inc. · Ophthalmic device
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Feb 1995
Decision
39d
Days
-
Risk

K946357 is an FDA 510(k) clearance for the COLLAGEN INTRACANALICULAR PLUG. Classified as Plug, Punctum (product code LZU).

Submitted by Oasis Medical, Inc. (Glendora, US). The FDA issued a Cleared decision on February 7, 1995 after a review of 39 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 Oasis Medical, Inc. devices

FDA 510(k) Submission Details - K946357

510(k) Number K946357 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 30, 1994
Decision Date February 07, 1995
Days to Decision 39 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
71d faster than avg
Panel avg: 110d · This submission: 39d
Pathway characteristics
Predicate-based equivalence.

LZU Device Classification - Class 0,

Product Code LZU Plug, Punctum
Device Class -

Regulatory Peers - LZU Plug, Punctum

All 8
Devices cleared under the same product code (LZU) and FDA review panel - the closest regulatory comparables to K946357.
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PDO Absorbable Punctum Plug
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VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}
K953394 · Visitec Co. · Oct 1995
VISITEC CANALICULAR STENT
K915809 · Visitec Co. · Feb 1992
LOOK TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT
K897190 · Look, Inc. · Mar 1990