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.

FDA 510(k) Regulatory Record - Brattle Instrument Corp.

7 devices

1-7 of 7