Bruel & Kjaer Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K901881 | VIBROMETRY SYSTEM | May 31, 1991 |
| K890446 | ANESTHETIC GAS MONITOR | August 11, 1989 |
| K827380 | SCANNER TYPE 1846 | July 9, 1982 |
| K827409 | REAL TIME ULTRASOUND SCANNER 1849 | July 9, 1982 |