8ch T/R Knee Coil
K-Number: K223225 · 2023-02-14
Device Summary
Frequently Asked Questions
What is the 8ch T/R Knee Coil?
8ch T/R Knee Coil is a medical device that received FDA 510(k) clearance on 2023-02-14. The listed applicant is Shenzhen RF Tech Co., Ltd.. The 510(k) number is K223225.
When did 8ch T/R Knee Coil receive FDA 510(k) clearance?
8ch T/R Knee Coil received FDA 510(k) clearance on 2023-02-14, under 510(k) number K223225.
Who is the listed applicant for 8ch T/R Knee Coil?
The FDA 510(k) record lists Shenzhen RF Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 8ch T/R Knee Coil?
The FDA product code for 8ch T/R Knee Coil is MOS.
Other records listing Shenzhen RF Tech Co., Ltd. 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.