Annes Daye, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Annes Daye, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Daye Tampon
1
Total
1
Cleared
0
Denied
Annes Daye, Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.
Last cleared in 2023. Active since 2023. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Annes Daye, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Annes Daye, Ltd.
1 devices