Nissel , Ltd. is one of 9887 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nissel , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: S-38 (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS, THE ESSTECH PS & SV (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS
2
Total
2
Cleared
0
Denied
Nissel , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 2 cleared submissions from 1992 to 1999. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Nissel , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nissel , Ltd.
2 devices