FDA 510(k)

VHA 放疗冲剂

K号: K222639 · 2022-11-04

决定日期2022-11-04

产品代码IXI

咨询委员会RA

决定实质等同

器械摘要

VHA Radiotherapy Bolus is the device name listed in this FDA 510(k) record. The listed applicant is Vha Dean. It received FDA 510(k) clearance on 2022-11-04 under 510(k) number K222639. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the VHA Radiotherapy Bolus?

VHA Radiotherapy Bolus is a medical device that received FDA 510(k) clearance on 2022-11-04. The listed applicant is Vha Dean. The 510(k) number is K222639.

When did VHA Radiotherapy Bolus receive FDA 510(k) clearance?

VHA Radiotherapy Bolus received FDA 510(k) clearance on 2022-11-04, under 510(k) number K222639.

Who is the listed applicant for VHA Radiotherapy Bolus?

The FDA 510(k) record lists Vha Dean as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VHA Radiotherapy Bolus?

The FDA product code for VHA Radiotherapy Bolus is IXI.

列明Vha Dean为申报人的其他记录

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