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Kontron Instruments, Inc.

FDA 510(k) & PMA Approved Devices — 57 products

Total Devices57
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K932268 MODIFICATIONS TO INTRA-AORTIC BALLOONSDSP1993-12-15 View
510(k) K925248 MODIFICATION OF INTRA-AORTIC BALLOON CATHETERSDSP1993-09-27 View
510(k) K923603 INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATIONDYB1993-03-08 View
510(k) K905313 KONTRON INTRA-AORTIC BALLOON PUMP, MODEL KAAT IIDSP1991-06-19 View
510(k) K903344 9.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)DSP1991-01-15 View
510(k) K896437 KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEMDPT1990-12-03 View
510(k) K892222 9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOONDSP1990-09-14 View
510(k) K882955 SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283DXN1990-01-26 View
510(k) K896386 MINIMON 7133B PATIENT MONITORDPS1989-12-13 View
510(k) K896417 KONTRON KOLORMON 7250 PATIENT MONITORDPS1989-12-12 View
510(k) K895425 MINIMON 7137B PATIENT MONITORDQA1989-09-26 View
510(k) K892799 8 FR PERCUTAN DOUBLE LUMEN INTRA-AORTIC BALLOONDSP1989-09-20 View
510(k) K892797 10 FR PERCUTAN DOUBLE LUMEN INTRA-AORTIC BALLOONDSP1989-09-20 View
510(k) K892798 9 FR PERCUTAN DOUBLE LUMEN INTRA-AORTIC BALLOONDSP1989-09-20 View
510(k) K892878 KONTRON INTRA-AORTIC BALLOON PUMP MODEL K9000DSP1989-09-13 View
510(k) K882206 SUPERMON ARRHYTHMIA MODULE 7270DSI1989-04-05 View
510(k) K882508 9.5 FRENCH PERCUTANEOUS DOUBLE LUMEN BALLOONDSP1989-03-20 View
510(k) K882274 10.5 FRENCH PERCUTANEOUS DOUBLE LUMEN INTRA-AORTICDSP1989-03-20 View
510(k) K890299 KONTRON PULSE OXIMETER 7840DQA1989-03-02 View
510(k) K883069 MINIMON 7134B PATIENT MONITORDRT1989-01-17 View
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