{"product_id":"fda-510k-k163512","title":"FDA 510(k) K163512, Zio AT ECG Monitoring System, by iRhythm Technologies, Inc.","description":"\u003cp\u003e\n\u003cstrong\u003eDevice Classification Name: \u003c\/strong\u003eOutpatient Cardiac Telemetry\u003cbr\u003e\n\u003cstrong\u003e510(k) Number: \u003c\/strong\u003eK163512\u003cbr\u003e\n\u003cstrong\u003eDevice Name:\u003c\/strong\u003e Zio AT ECG Monitoring System\u003cbr\u003e\n\u003cstrong\u003eApplicant:\u003c\/strong\u003e iRhythm Technologies, Inc.\u003cbr\u003e\n\u003cstrong\u003eRegulation Number: \u003c\/strong\u003e870.1025\u003cbr\u003e\n\u003cstrong\u003eClassification Product Code: \u003c\/strong\u003eQYX\u003cbr\u003e\n\u003cstrong\u003eDate Received: \u003c\/strong\u003e12\/15\/2016\u003cbr\u003e\n\u003cstrong\u003eDecision Date:\u003c\/strong\u003e 06\/02\/2017\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\u003eCardiovascular\u003cbr\u003e\n\u003c\/p\u003e\n\u003cp\u003e\n\u003cstrong\u003eTotal number of pages:\u003c\/strong\u003e 2,996\u003cbr\u003e\n\u003cstrong\u003eFully redacted pages:\u003c\/strong\u003e 1\u003cbr\u003e\n\u003cstrong\u003eContent pages:\u003c\/strong\u003e 2,995\n\u003c\/p\u003e","brand":"FDA","offers":[{"title":"Default Title","offer_id":51310822588580,"sku":"FDA510K163512","price":3500.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-510k-k163512","provider":"FOIA Document Source","version":"1.0","type":"link"}