Surgical Instrument Systems (Sis), Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgical Instrument Systems (Sis), Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Surgical Instrument Systems (Sis), Ltd. has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Surgical Instrument Systems (Sis), Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgical Instrument Systems (Sis), Ltd.
1 devices