Skip to content

FDA.reportPublic FDA data

NDC RxNorm DailyMed Applications GUDID GMDN PMA PMN MAUDE Recalls

Search FDA.report

Home
PMN
K183358

510(k) K183358

Device: K183358
510(k) number: K183358

FDA.report indexes public FDA datasets and legacy FDA.report records. Source data can change; verify critical regulatory decisions with the official FDA source.

Sitemap Robots Ads.txt