Medical Device Manufacturer · US , Mchenry , IL

Baurs Krey Assoc., Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 1984

Total

Cleared

Denied

Baurs Krey Assoc., Inc. has 3 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 3 cleared submissions from 1984 to 1984. Primary specialty: General Hospital.

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

Baurs Krey Assoc., Inc. 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 - Baurs Krey Assoc., Inc.

4 devices

1-4 of 4