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K-Lok, Inc.

2 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
K-LOK CATHETER SECUREMENT DEVICE MODIFICATION (K935252)K-Lok, Inc.1994-02-18
K-LOK CATHETER SECUREMENT DEVICE (K930225)K-Lok, Inc.1993-04-21

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Every clearance here is in the API, with alerts when new ones post.