Perstorp AB C/O Robert Joel Slomoff - FDA 510(k) Cleared Devices
2
Total
1
Cleared
0
Denied
Perstorp AB C/O Robert Joel Slomoff has 1 FDA 510(k) cleared medical devices. Based in Potomac, US.
Historical record: 1 cleared submissions from 1987 to 1991. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Perstorp AB C/O Robert Joel Slomoff Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Perstorp AB C/O Robert Joel Slomoff
2 devices