Electro-Kinetic Eng/Mfg is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Electro-Kinetic Eng/Mfg - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Electro-Kinetic Eng/Mfg has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 1 cleared submissions from 1981 to 1981. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Electro-Kinetic Eng/Mfg Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Electro-Kinetic Eng/Mfg
1 devices