Partnership Medical Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Partnership Medical Limited - FDA 510(k) Cleared Devices
Recent clearances: ScopeFlow Pure(TM), EndoStream(TM)
2
Total
2
Cleared
0
Denied
Partnership Medical Limited has 2 FDA 510(k) cleared medical devices. Based in Fenton, GB.
Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Partnership Medical Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qrc Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Partnership Medical Limited
2 devices