Seiler Precision Microscopes is one of 21843 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seiler Precision Microscopes - FDA 510(k) Cleared Devices
Recent clearances: SEILER COLPOSCOPE, MODELS 935, 955 AND 985
1
Total
1
Cleared
0
Denied
Seiler Precision Microscopes has 1 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Seiler Precision Microscopes Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seiler Precision Microscopes
1 devices