Medical Device Manufacturer · US , Mchenry , IL

Brattle Instrument Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1977

Total

Cleared

Denied

Brattle Instrument Corp. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1977 to 1981. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Brattle Instrument Corp. Filter by specialty or product code using the sidebar.

Brattle Instrument Corp. 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 - Brattle Instrument Corp.

7 devices

1-7 of 7