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Bruel & Kjaer Industri A/S

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K914945 DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535, MODIFIEDIYO1992-06-26 View
510(k) K875357 BIOPSY FIXATION UNIT-TYPE UA 0997IYO1988-07-01 View
510(k) K852502 AMENDMENT ULTRASOUND SCANNER TYPE 1842/1846/1849IYO1986-10-23 View
510(k) K842090 RHINO-LARYNX STROBOSCOPE TYPE 4914EQL1984-07-18 View
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