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K-Lok, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K935252 K-LOK CATHETER SECUREMENT DEVICE MODIFICATIONKMK1994-02-18 View
510(k) K930225 K-LOK CATHETER SECUREMENT DEVICEKMK1993-04-21 View
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