FDA 510(k)

VHA Radiotherapy Bolus

K-Number: K222639 · 2022-11-04

Decision Date2022-11-04

Product CodeIXI

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Other records listing Vha Dean 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.

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Official Source

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