# Brattle Instrument Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 7 (1977–1981): 7 510(k) clearances
- Product codes: HGM (3), KLK (1), IXQ (1), IXO (1), HGI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K810588: Synchronizer #208 (Apr 10, 1981)
- K802978: Transcutaneous Blood Oxygen Monitor #300 (Feb 2, 1981)
- K781681: Phipiological Synchronizer Part#205 (Oct 17, 1978)
- K770692: Monitor, Fetal, NO. L04-1100 (Apr 26, 1977)
- K770296: Fetal Monitor, Part #101-11009 (Mar 9, 1977)
- K770295: Abdominal Ecg Processor for Fetal Moni. (Mar 9, 1977)
- K770297: Fetal Monitor, Part #100-11009 (Mar 9, 1977)

Source page: https://510kreport.com/company/brattle-instrument