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Triton Technology, Inc.

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

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K932142 SUCTION GUILLOTINE DEVICEFCK1993-09-24 View
510(k) K911448 MULTIPLE BIOPSY DEVICE-MBXFCK1991-04-16 View
510(k) K902883 TISSUE/POLYP TRAP SYSTEMBYZ1990-09-12 View
510(k) K881303 TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETERDPT1988-11-29 View
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