Westar Medical Products, Inc. is one of 21653 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Westar Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WESTAR SERIES DENTAL UNITS
1
Total
1
Cleared
0
Denied
Westar Medical Products, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mukilteo, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Westar Medical Products, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Westar Medical Products, Inc.
1 devices