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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 35 of 35 Results
510(K) Number: K181166
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Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2... 2 01/04/2024 FEI # 2518422
Philips Respironics, Inc.
Trilogy Evo, Evo Clinical Korean (1137823) and Evo Caregiver Korean (1137853) Instructions for Use 2 07/07/2023 FEI # 2518422
Philips Respironics, Inc.
Trilogy Evo, Product numbers BL2110X15B, CA2110X12B, DE2110X13B, DS2110X11B, EE2110X15B, ES2110X15B,... 2 08/13/2021 FEI # 2518422
Philips Respironics, Inc.
Trilogy Evo O2, Product numbers DE2100X13B, DS2100X11B, EE2100X15B, ES2100X15B, EU2100X15B, FR2100X1... 2 08/13/2021 FEI # 2518422
Philips Respironics, Inc.
Trilogy EV300, Product numbers CA2200X12B, DS2200X11B, FX2200X15B, IN2200X15B 2 08/13/2021 FEI # 2518422
Philips Respironics, Inc.
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