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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K242225
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Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation... 1 09/26/2025 Medline Industries, LP
Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic ... 1 02/06/2026 Medline Industries, LP
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