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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K181311
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Philips Interventional Hemodynamic Application R.1.2X, R.1.3.0, R1.2.1. Software that enables invasi... 2 05/30/2024 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Hemodynamic Application, Model Number 722463, Software Version Number: R1.2.2 and R1.2.3. F... 2 05/06/2022 Philips North America Llc
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