{"product_id":"fda-510k-k190269","title":"FDA 510(k) K190269, PureLift, by Xtreem Pulse, LLC","description":"\u003cp\u003e\n\u003cstrong\u003eDevice Classification Name: \u003c\/strong\u003eStimulator, Transcutaneous Electrical, Aesthetic Purposes\u003cbr\u003e\n\u003cstrong\u003e510(k) Number: \u003c\/strong\u003eK190269\u003cbr\u003e\n\u003cstrong\u003eDevice Name:\u003c\/strong\u003e PureLift\u003cbr\u003e\n\u003cstrong\u003eApplicant:\u003c\/strong\u003e Xtreem Pulse, LLC\u003cbr\u003e\n\u003cstrong\u003eRegulation Number: \u003c\/strong\u003e882.5890\u003cbr\u003e\n\u003cstrong\u003eClassification Product Code: \u003c\/strong\u003eNFO\u003cbr\u003e\n\u003cstrong\u003eDate Received: \u003c\/strong\u003e02\/08\/2019\u003cbr\u003e\n\u003cstrong\u003eDecision Date:\u003c\/strong\u003e 08\/28\/2019\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 1,756\u003cbr\u003e\n\u003cstrong\u003eFully redacted pages:\u003c\/strong\u003e 909\u003cbr\u003e\n\u003cstrong\u003eContent pages:\u003c\/strong\u003e 847\n\u003c\/p\u003e","brand":"FDA","offers":[{"title":"Default Title","offer_id":51313221009572,"sku":"FDA510K190269","price":1996.27,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-510k-k190269","provider":"FOIA Document Source","version":"1.0","type":"link"}