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Laurus Medical Corp.

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

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K973415 CURVILINEAR SUTURE PLACEMENT SYSTEMGCJ1997-12-02 View
510(k) K973215 STEREOTACTIC NEEDLE CORE BIOPSY SYSTEMKNW1997-11-06 View
510(k) K960317 LAURUS NEEDLE CORE BIOPSY SYSTEMFCG1996-03-15 View
510(k) K932553 DISPOSABLE SUTURE PLACEMENT SYSTEMGCJ1994-05-12 View
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