Tis, Inc. is one of 25808 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Tis, Inc. has 1 FDA 510(k) cleared medical devices. Based in Marietta, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Tis, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Tis, Inc.
1 devices