Skip to content

FDA.reportPublic FDA data

NDC RxNorm DailyMed Applications GUDID GMDN PMA PMN MAUDE Recalls

Search FDA.report

Home
PMN
DK790105

510(k) DK790105

Device: Automated Blood Cell Separator -filtration: Terumo Imugard
Applicant: Terumo Corporation
510(k) number: DK790105
Decision date: 1979-05-24

Related Records#

Company: Terumo Corporation

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

Privacy Sitemap Robots Ads.txt