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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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