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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K203060
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VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF) 2 07/28/2023 Johnson & Johnson Surgical Vision, Inc.
Veritas Advanced Infusion Packs, REF: VRT-AI 2 01/20/2023 Johnson & Johnson Surgical Vision, Inc.
Veritas Advanced Infusion Packs. Used in ophthalmic procedures. 2 10/12/2022 Johnson & Johnson Surgical Vision, Inc.
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