Northstar Healthcare Holdings Limited is one of 16447 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Northstar Healthcare Holdings Limited - FDA 510(k) Cleared Devices
Recent clearances: POWDER FREE LATEX PATIENT EXAM GLOVE WITH PROTEIN LABELING CLAIM (50 MICROGRAMS PER DM SQUARED OR LESS OF WATER SOLUBLE
1
Total
1
Cleared
0
Denied
Northstar Healthcare Holdings Limited has 1 FDA 510(k) cleared medical devices. Based in Mc Henry, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Northstar Healthcare Holdings Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Northstar Healthcare Holdings Limited
1 devices