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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K081718
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FDA Recall
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Ocean Water Seal Chest Drain, Single Collection W/AC, P/N: 2002-000 2 06/29/2015 Atrium Medical Corporation
Ocean Water Seal Chest Drain, SINGLE W/AC P/N: 2002-100 2 06/29/2015 Atrium Medical Corporation
Oasis Dry Suction Water Seal Chest Drain, DRY SINGLE W/AC P/N: 3600-100 2 06/29/2015 Atrium Medical Corporation
EXPRESS Dry Seal Chest Drain, Single Collection P/N: 4000-100N 2 06/29/2015 Atrium Medical Corporation
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