K973872 is an FDA 510(k) clearance for the ATRION MEDICAL COATED LACRIMAL INTUBATION SET. Classified as Lacrimal Stents And Intubation Sets (product code OKS).
Submitted by Atrion Medical Products, Inc. (Arab, US). The FDA issued a Cleared decision on January 8, 1998 after a review of 90 days - within the typical 510(k) review window.
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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Ophthalmic review framework, consistent with the majority of Class II 510(k) submissions.
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