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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K915390
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Baxter Interlink System Non-DEHP Standard Bore 3-Lead Catheter Extension Set, product code 2N3335; A... 2 03/24/2006 FEI # 1416980
Baxter Healthcare Corp.
Baxter Interlink System 3-Lead Extension Set, product code 1C8442; An Rx sterile, nonpyrogenic fluid... 2 03/24/2006 FEI # 1416980
Baxter Healthcare Corp.
Baxter Microbore 3-Lead Extension Set with 0.22 Micron High Pressure Pediatric Filter, catalog 2N334... 1 02/06/2003 FEI # 1416980
Baxter Healthcare Corp.
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