Bruel & Kjaer Industri A/S

Bruel & Kjaer Industri A/S holds 4 FDA 510(k) medical device clearances, first cleared 1984, most recent 1992.

Top product codes for Bruel & Kjaer Industri A/S

IYO — Radiology3 devices
EQL — Ear, Nose, Throat1 device

Recent clearances by Bruel & Kjaer Industri A/S

K914945 — DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535, MODIFIEDCode IYO·1992-06-26
K875357 — BIOPSY FIXATION UNIT-TYPE UA 0997Code IYO·1988-07-01
K852502 — AMENDMENT ULTRASOUND SCANNER TYPE 1842/1846/1849Code IYO·1986-10-23
K842090 — RHINO-LARYNX STROBOSCOPE TYPE 4914Code EQL·1984-07-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.