Intervene Group, Ltd. is one of 463 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Intervene Group, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DASH 6 NRFit Lock Syringe + Accessories, DASH 6 NRFit Slip Syringe + Accessories, DASH 6 NRFit Plastic LOR Syringe + Accessories
1
Total
1
Cleared
0
Denied
Intervene Group, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Uxbridge, GB.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Intervene Group, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The Weinberg Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Intervene Group, Ltd.
1 devices