Northstar Healthcare Holdings is one of 88 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Northstar Healthcare Holdings - FDA 510(k) Cleared Devices
Recent clearances: BLUE STERILE POWDER FREE NITRILE EXAMINATION GLOVE, TEXTURED, NATURAL TO OFF-WHITE, LATEX, STERILE, POWDER FREE EXAMINATION GLOVES, WITH PROTEIN LABELING CLAIM (50 UG/DM2 O, TEXTURED, BLUE, LATEX, POWDER FREE EXAMINATION GLVOES, WITH PROTEIN LABELING CLAIM (50UG/DM OR LESS OF WATER SOLUBLE PRO
Northstar Healthcare Holdings has 9 FDA 510(k) cleared medical devices. Based in Dublin 2, IE.
Historical record: 9 cleared submissions from 2012 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Northstar Healthcare Holdings Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.