Mti Corp./ Electrostar S.A.-Haiti is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mti Corp./ Electrostar S.A.-Haiti - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Mti Corp./ Electrostar S.A.-Haiti has 1 FDA 510(k) cleared medical devices. Based in Safety Harbor, US.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mti Corp./ Electrostar S.A.-Haiti Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mti Corp./ Electrostar S.A.-Haiti
1 devices