Chitogel, Ltd. is one of 29 FDA 510(k) medical device manufacturers from New Zealand in the dataset, ranked by real submission volume.
Chitogel, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Chitogel Endoscopic Sinus Surgery Kit
1
Total
1
Cleared
0
Denied
Chitogel, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Dunedin, NZ.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Chitogel, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Strategies, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Chitogel, Ltd.
1 devices