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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K811627
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Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000 1 06/13/2026 FEI # 3013162291
ARROW INTERNATIONAL, LLC
Peritoneal Lavage Kits, Model number AK-09000 2 08/25/2004 FEI # 3015859709
Arrow International Inc
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