Premco Medical Systems, Inc. is one of 23530 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Premco Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PRODIGY NPWT SYSTEM MODEL PRODIGY 800V
1
Total
1
Cleared
0
Denied
Premco Medical Systems, Inc. has 1 FDA 510(k) cleared medical devices. Based in New Rochelle, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Premco Medical Systems, Inc. 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 - Premco Medical Systems, Inc.
1 devices