Qualtex, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Qualtex, Inc. has 2 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 2 cleared submissions from 1978 to 1990. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Qualtex, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Qualtex, Inc.
2 devices