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FDA 510(k)

8ch Wrist Coil

K-Number: K222325 · 2022-08-31

Decision Date2022-08-31
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

8ch Wrist Coil is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corporation (Business Trade Name: Philips). It received FDA 510(k) clearance on 2022-08-31 under 510(k) number K222325. 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 8ch Wrist Coil?

8ch Wrist Coil is a medical device that received FDA 510(k) clearance on 2022-08-31. The listed applicant is Invivo Corporation (Business Trade Name: Philips). The 510(k) number is K222325.

When did 8ch Wrist Coil receive FDA 510(k) clearance?

8ch Wrist Coil received FDA 510(k) clearance on 2022-08-31, under 510(k) number K222325.

Who is the listed applicant for 8ch Wrist Coil?

The FDA 510(k) record lists Invivo Corporation (Business Trade Name: Philips) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 8ch Wrist Coil?

The FDA product code for 8ch Wrist Coil is MOS.

Other records listing Invivo Corporation (Business Trade Name: Philips) as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: MOS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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