Medical Device Manufacturer · CA , Canada L4v 1p1

Allelix Diagnostics, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

Total

Cleared

Denied

Allelix Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Canada L4v 1p1, CA.

Historical record: 2 cleared submissions from 1988 to 1989. Primary specialty: Microbiology.

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

Allelix Diagnostics, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Allelix Diagnostics, Inc.

2 devices

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