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Bruel & Kjaer Industri A/S

FDA Regulatory Profile

Bruel & Kjaer Industri A/S appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 26, 1992.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K914945DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535, MODIFIEDJune 26, 1992
K875357BIOPSY FIXATION UNIT-TYPE UA 0997July 1, 1988
K852502AMENDMENT ULTRASOUND SCANNER TYPE 1842/1846/1849October 23, 1986
K842090RHINO-LARYNX STROBOSCOPE TYPE 4914July 18, 1984

FDA data resources