FDA 510(k)

Helios+ UV-C System

Номер K: K242604 · 2025-05-27

ЗаявительPreventamed Technologies, Inc. Dba Surfacide Manufacturing

Дата решения2025-05-27

Код продуктаQXJ

Консультативный комитетHO

РешениеSubstantially Equivalent

Описание устройства

Helios+ UV-C System is the device name listed in this FDA 510(k) record. The listed applicant is Preventamed Technologies, Inc. Dba Surfacide Manufacturing. It received FDA 510(k) clearance on 2025-05-27 under 510(k) number K242604. The device is classified under product code QXJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the Helios+ UV-C System?

Helios+ UV-C System is a medical device that received FDA 510(k) clearance on 2025-05-27. The listed applicant is Preventamed Technologies, Inc. Dba Surfacide Manufacturing. The 510(k) number is K242604.

When did Helios+ UV-C System receive FDA 510(k) clearance?

Helios+ UV-C System received FDA 510(k) clearance on 2025-05-27, under 510(k) number K242604.

Who is the listed applicant for Helios+ UV-C System?

The FDA 510(k) record lists Preventamed Technologies, Inc. Dba Surfacide Manufacturing as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Helios+ UV-C System?

The FDA product code for Helios+ UV-C System is QXJ.

Связанные клинические исследования

Связанные записи сопоставляются автоматически на основании названий, кодов продукции или иных метаданных. Сопоставление не подтверждает клиническую, научную, корпоративную или регуляторную связь; ознакомьтесь с официальными источниками по ссылкам.

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