ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-4000
Feb 1999
61d
Intracom Corp.
1
Total
1
Cleared
0
Denied
Intracom Corp. — FDA 510(k) Submissions
Intracom Corp. has submitted 1 FDA 510(k) premarket notifications since 1999, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Device, Digital Image Storage, Radiological . Use the specialty filter in the sidebar to narrow results.
1 devices