1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil
K-Number: K222257 · 2022-08-23
Device Summary
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.