{"product_id":"fda-510k-k201271","title":"FDA 510(k) K201271, Benchmark BMX96 Access System, by Penumbra, Inc.","description":"\u003cp\u003e\n\u003cstrong\u003eDevice Classification Name: \u003c\/strong\u003eCatheter, Percutaneous\u003cbr\u003e\n\u003cstrong\u003e510(k) Number: \u003c\/strong\u003eK201271\u003cbr\u003e\n\u003cstrong\u003eDevice Name:\u003c\/strong\u003e Benchmark BMX96 Access System\u003cbr\u003e\n\u003cstrong\u003eApplicant:\u003c\/strong\u003e Penumbra, Inc.\u003cbr\u003e\n\u003cstrong\u003eRegulation Number: \u003c\/strong\u003e870.125\u003cbr\u003e\n\u003cstrong\u003eClassification Product Code: \u003c\/strong\u003eDQY\u003cbr\u003e\n\u003cstrong\u003eDate Received: \u003c\/strong\u003e2020-05-12\u003cbr\u003e\n\u003cstrong\u003eDecision Date:\u003c\/strong\u003e 2020-06-11\u003cbr\u003e\n\u003cstrong\u003eDecision:\u003c\/strong\u003e Substantially Equivalent (SESE)\u003cbr\u003e\n\u003cstrong\u003eRegulation Medical Specialty: \u003c\/strong\u003eCardiovascular\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 453\u003cbr\u003e\n\u003cstrong\u003eFully redacted pages:\u003c\/strong\u003e 288\u003cbr\u003e\n\u003cstrong\u003eContent pages:\u003c\/strong\u003e 165\n\u003c\/p\u003e","brand":"FDA","offers":[{"title":"Default Title","offer_id":51315379536036,"sku":"FDA510K201271","price":571.33,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-510k-k201271","provider":"FOIA Document Source","version":"1.0","type":"link"}