Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

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

K-Number: K222257 · 2022-08-23

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 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 2022-08-23 under 510(k) 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. The listed applicant is Invivo Corporation (Business Trade Name: Philips). The 510(k) number is K222257.

When did 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil receive FDA 510(k) clearance?

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

Who is the listed applicant for 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee 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 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 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

View on FDA Database →

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