Resect Medical, Inc. is one of 24544 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Resect Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RESECT MEDICAL INLINE BI-POLAR RF LINEAR COAGULATION DEVICE
1
Total
1
Cleared
0
Denied
Resect Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Fremont, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Resect Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kema Quality B.V. as regulatory consultant.
FDA 510(k) Regulatory Record - Resect Medical, Inc.
1 devices