{"product_id":"fda-510k-k954255","title":"FDA 510(k) K954255 Summary, PHILIPS TOMOSCAN SR 8000, by Philips Medical Systems North America, Inc.","description":"\u003cp\u003e\u003cstrong\u003eNOTE: Summary of Safety and Effectiveness Document Only\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eDevice Classification Name: \u003c\/strong\u003eSystem, X-Ray, Tomography, Computed\u003cbr\u003e\u003cstrong\u003e510(k) Number: \u003c\/strong\u003eK954255\u003cbr\u003e\u003cstrong\u003eDevice Name:\u003c\/strong\u003e PHILIPS TOMOSCAN SR 8000\u003cbr\u003e\u003cstrong\u003eApplicant:\u003c\/strong\u003e Philips Medical Systems North America, Inc.\u003cbr\u003e\u003cstrong\u003eRegulation Number: \u003c\/strong\u003e892.1750\u003cbr\u003e\u003cstrong\u003eClassification Product Code: \u003c\/strong\u003eJAK\u003cbr\u003e\u003cstrong\u003eDate Received: \u003c\/strong\u003e09\/11\/1995\u003cbr\u003e\u003cstrong\u003eDecision Date:\u003c\/strong\u003e 10\/07\/1995\u003cbr\u003e\u003cstrong\u003eDecision:\u003c\/strong\u003e Substantially Equivalent (SESE)\u003cbr\u003e\u003cstrong\u003eRegulation Medical Specialty: \u003c\/strong\u003eRadiology\u003cbr\u003e\u003cstrong\u003e510k Review Panel: \u003c\/strong\u003eRadiology\u003cbr\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eTotal number of pages:\u003c\/strong\u003e 1\u003cbr\u003e\u003cstrong\u003eFully redacted pages:\u003c\/strong\u003e 0\u003cbr\u003e\u003cstrong\u003eContent pages:\u003c\/strong\u003e 1\u003c\/p\u003e","brand":"FDA","offers":[{"title":"Default Title","offer_id":51315066110116,"sku":"FDA510K954255","price":175.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/foiadocs.com\/products\/fda-510k-k954255","provider":"FOIA Document Source","version":"1.0","type":"link"}