K962151 is an FDA 510(k) clearance for the RYDER LACRIMAL INTUBATIONSET. Classified as Lacrimal Stents And Intubation Sets (product code OKS).
Submitted by Ryder Intl. Corp. (Arab, US). The FDA issued a Cleared decision on September 18, 1996 after a review of 106 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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