{"product_id":"fda-510k-k142567","title":"FDA 510(k) K142567, RETeval Visual Electrodiagnostic Device, by Lkc Technologies, Inc.","description":"\u003cp\u003e\n\u003cstrong\u003eDevice Classification Name: \u003c\/strong\u003eStimulator, Photic, Evoked Response\u003cbr\u003e\n\u003cstrong\u003e510(k) Number: \u003c\/strong\u003eK142567\u003cbr\u003e\n\u003cstrong\u003eDevice Name:\u003c\/strong\u003e RETeval Visual Electrodiagnostic Device\u003cbr\u003e\n\u003cstrong\u003eApplicant:\u003c\/strong\u003e Lkc Technologies, Inc.\u003cbr\u003e\n\u003cstrong\u003eRegulation Number: \u003c\/strong\u003e882.1890\u003cbr\u003e\n\u003cstrong\u003eClassification Product Code: \u003c\/strong\u003eGWE\u003cbr\u003e\n\u003cstrong\u003eDate Received: \u003c\/strong\u003e09\/12\/2014\u003cbr\u003e\n\u003cstrong\u003eDecision Date:\u003c\/strong\u003e 05\/19\/2015\u003cbr\u003e\n\u003cstrong\u003eDecision:\u003c\/strong\u003e Substantially Equivalent (SESE)\u003cbr\u003e\n\u003cstrong\u003eRegulation Medical Specialty: \u003c\/strong\u003eNeurology\u003cbr\u003e\n\u003cstrong\u003e510k Review Panel: \u003c\/strong\u003eNeurology\u003cbr\u003e\n\u003c\/p\u003e\n\u003cp\u003e\n\u003cstrong\u003eTotal number of pages:\u003c\/strong\u003e 2,960\u003cbr\u003e\n\u003cstrong\u003eFully redacted pages:\u003c\/strong\u003e 2,040\u003cbr\u003e\n\u003cstrong\u003eContent pages:\u003c\/strong\u003e 920\n\u003c\/p\u003e","brand":"FDA","offers":[{"title":"Default Title","offer_id":51310822359204,"sku":"FDA510K142567","price":2142.75,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-510k-k142567","provider":"FOIA Document Source","version":"1.0","type":"link"}