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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K161313
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ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch di... 2 10/19/2022 FEI # 3013162291
ARROW INTERNATIONAL Inc.
Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS 2 06/16/2019 FEI # 3015859709
Arrow International Inc
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