Brattle Instrument Corp.
Brattle Instrument Corp. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 10, 1981.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K810588 | SYNCHRONIZER #208 | April 10, 1981 |
| K802978 | TRANSCUTANEOUS BLOOD OXYGEN MONITOR #300 | February 2, 1981 |
| K781681 | PHIPIOLOGICAL SYNCHRONIZER PART#205 | October 17, 1978 |
| K770692 | MONITOR, FETAL, NO. L04-1100 | April 26, 1977 |
| K770296 | FETAL MONITOR, PART #101-11009 | March 9, 1977 |
| K770295 | ABDOMINAL ECG PROCESSOR FOR FETAL MONI. | March 9, 1977 |
| K770297 | FETAL MONITOR, PART #100-11009 | March 9, 1977 |