Bruel & Kjaer Instruments, Inc.

FDA Regulatory Profile

Bruel & Kjaer Instruments, Inc. 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 May 31, 1991.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K901881VIBROMETRY SYSTEMMay 31, 1991
K890446ANESTHETIC GAS MONITORAugust 11, 1989
K827380SCANNER TYPE 1846July 9, 1982
K827409REAL TIME ULTRASOUND SCANNER 1849July 9, 1982