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This site had the following in the web page, "This website contains over 132,000 FDA 510k applications and decisions collected since May, 1976 from the U." We observed that the web site stated " Food and Drug Administrations publicly available databases of FDA Device Approvals and Clearances." It also stated " Additionally, we have provided convenient cross-linking of records by applicant company name, contact name, device classification, and product code. Things You Can Do With This Website. Check the status of an FDA 510k Application by browsing to it by company name." The header had submissions as the highest ranking keyword. It was followed by 510k, cdrh, and device approvals and clearances which isn't as ranked as highly as submissions. The next words the site uses is premarket notification. fda 510k approval was also included and could not be understood by search engines.