Bruel & Kjaer Industri A/S
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K914945 | DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535, MODIFIED | June 26, 1992 |
| K875357 | BIOPSY FIXATION UNIT-TYPE UA 0997 | July 1, 1988 |
| K852502 | AMENDMENT ULTRASOUND SCANNER TYPE 1842/1846/1849 | October 23, 1986 |
| K842090 | RHINO-LARYNX STROBOSCOPE TYPE 4914 | July 18, 1984 |