Medical Device Manufacturer · CA , Kitchener Ontario

Diva International, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

Total

Cleared

Denied

Diva International, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kitchener Ontario, CA.

Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Obstetrics & Gynecology.

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

Diva International, 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 - Diva International, Inc.

1 devices

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