Technolab Industries (Canada) , Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Technolab Industries (Canada) , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Technolab Industries (Canada) , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Montreal, Quebec, CA.
Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Technolab Industries (Canada) , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Technolab Industries (Canada) , Ltd.
1 devices