FDA 510(k) Applications Submitted by Invivo Corporation (Business Trade Name: Philips)

FDA 510(k) Number Submission Date Device Name Applicant
K213727 11/26/2021 dS Sentinelle Breast 16ch 3.0T Coil Invivo Corporation (Business Trade Name: Philips)
K213735 11/29/2021 dS Sentinelle Breast 16ch 1.5T Coil Invivo Corporation (Business Trade Name: Philips)
K222257 07/27/2022 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil Invivo Corporation (Business Trade Name: Philips)
K222325 08/02/2022 8ch Wrist Coil Invivo Corporation (Business Trade Name: Philips)
K232762 09/08/2023 dS Breast Coil 7ch 1.5T Invivo Corporation (Business Trade Name: Philips)
K213351 10/08/2021 ds Head 32ch 3.0T Invivo Corporation (Business Trade Name: Philips)


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