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The Kendall Company, L.P.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K990530 KERLIX MD ANTIMICROBIAL GAUZE DRESSINGNAD2000-01-31 View
510(k) K992079 KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325JOW1999-09-29 View
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