Medical Device Manufacturer · US , Brier , WA

Keema and Co. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Keema and Co. has 1 FDA 510(k) cleared medical devices. Based in Brier, US.

Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Keema and Co. Filter by specialty or product code using the sidebar.

Keema and Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Keema and Co.

1 devices

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