Medical Device Manufacturer · CA , K8n 5b6

Anetec, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989
2
Total
2
Cleared
0
Denied

Anetec, Inc. has 2 FDA 510(k) cleared medical devices. Based in K8n 5b6, CA.

Historical record: 2 cleared submissions from 1989 to 1994. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Anetec, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Anetec, Inc.
2 devices
1-2 of 2
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