FDA 510(k)

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

K番号: K222257 · 2022-08-23

申請者Invivo Corporation (Business Trade Name: Philips)

決定日2022-08-23

製品コードMOS

諮問委員会RA （注：由于原文中未提供具体的医疗设备监管文本内容，因此无法进行翻译。请提供具体的文本内容以便进行翻译。）

決定大幅同等

医療機器の概要

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.

よくある質問

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.

申請者としてInvivo Corporation (Business Trade Name: Philips)を記載するその他の記録

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