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FDA 510(k)

1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil

K-Number: K222257 · 2022-08-23

ApplicantInvivo Corporation (Business Trade Name: Philips)
Decision Date2022-08-23
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil is a medical device manufactured by Invivo Corporation (Business Trade Name: Philips). It received FDA 510(k) clearance on 2022-08-23 under approval number K222257. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil?

1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil is a medical device that received FDA 510(k) clearance on 2022-08-23. It is manufactured by Invivo Corporation (Business Trade Name: Philips). The 510(k) number is K222257.

When was 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil approved by the FDA?

1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil received FDA 510(k) clearance on 2022-08-23, under approval number K222257.

What company makes 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil?

1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil is manufactured by Invivo Corporation (Business Trade Name: Philips).

What is the FDA product code for 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil?

The FDA product code for 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil is MOS.

Other Devices by Invivo Corporation (Business Trade Name: Philips)

K213351ds Head 32ch 3.0T K2223258ch Wrist Coil K213735dS Sentinelle Breast 16ch 1.5T Coil K213727dS Sentinelle Breast 16ch 3.0T Coil K232762dS Breast Coil 7ch 1.5T

Related Devices (Code: MOS)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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