{"product_id":"fda-510k-k030315","title":"FDA 510(k) K030315, MODIFICATION TO ULTROID HEMORRHOID MANAGEMENT SYSTEM, by Ultroid, LLC","description":"\u003cp\u003e\n\u003cstrong\u003eDevice Classification Name: \u003c\/strong\u003eUnit, Electrosurgical, Endoscopic (With Or Without Accessories)\u003cbr\u003e\n\u003cstrong\u003e510(k) Number: \u003c\/strong\u003eK030315\u003cbr\u003e\n\u003cstrong\u003eDevice Name:\u003c\/strong\u003e MODIFICATION TO ULTROID HEMORRHOID MANAGEMENT SYSTEM\u003cbr\u003e\n\u003cstrong\u003eApplicant:\u003c\/strong\u003e Ultroid, LLC\u003cbr\u003e\n\u003cstrong\u003eRegulation Number: \u003c\/strong\u003e876.4300\u003cbr\u003e\n\u003cstrong\u003eClassification Product Code: \u003c\/strong\u003eKNS\u003cbr\u003e\n\u003cstrong\u003eDate Received: \u003c\/strong\u003e01\/30\/2003\u003cbr\u003e\n\u003cstrong\u003eDecision Date:\u003c\/strong\u003e 02\/27\/2003\u003cbr\u003e\n\u003cstrong\u003eDecision:\u003c\/strong\u003e Substantially Equivalent (SESE)\u003cbr\u003e\n\u003cstrong\u003eRegulation Medical Specialty: \u003c\/strong\u003eGastroenterology\/Urology\u003cbr\u003e\n\u003cstrong\u003e510k Review Panel: \u003c\/strong\u003eGastroenterology\/Urology\u003cbr\u003e\n\u003c\/p\u003e\n\u003cp\u003e\n\u003cstrong\u003eTotal number of pages:\u003c\/strong\u003e 114\u003cbr\u003e\n\u003cstrong\u003eFully redacted pages:\u003c\/strong\u003e 0\u003cbr\u003e\n\u003cstrong\u003eContent pages:\u003c\/strong\u003e 114\n\u003c\/p\u003e","brand":"FDA","offers":[{"title":"Default Title","offer_id":51310185218212,"sku":"FDA510K030315","price":419.04,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-510k-k030315","provider":"FOIA Document Source","version":"1.0","type":"link"}