Hightech Development - FDA 510(k) Cleared Devices
Recent clearances: Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE
1
Total
1
Cleared
0
Denied
Hightech Development has 1 FDA 510(k) cleared medical devices. Based in Prague, CZ.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Hightech Development Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hightech Development
1 devices