FDA 510(k)

Perin Health System (PHD80060-2)

Номер K: K252984 · 2026-01-22

Дата решения2026-01-22

Код продуктаDRG

Консультативный комитетCV

РешениеSubstantially Equivalent

Описание устройства

Perin Health System (PHD80060-2) is the device name listed in this FDA 510(k) record. The listed applicant is Perin Health Devices, LLC. It received FDA 510(k) clearance on 2026-01-22 under 510(k) number K252984. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the Perin Health System (PHD80060-2)?

Perin Health System (PHD80060-2) is a medical device that received FDA 510(k) clearance on 2026-01-22. The listed applicant is Perin Health Devices, LLC. The 510(k) number is K252984.

When did Perin Health System (PHD80060-2) receive FDA 510(k) clearance?

Perin Health System (PHD80060-2) received FDA 510(k) clearance on 2026-01-22, under 510(k) number K252984.

Who is the listed applicant for Perin Health System (PHD80060-2)?

The FDA 510(k) record lists Perin Health Devices, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Perin Health System (PHD80060-2)?

The FDA product code for Perin Health System (PHD80060-2) is DRG.

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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Связанные устройства (Код: DRG)

K261569UbiqVue™ 2AYe Cardiac System (UX2253)Lifesignals, Inc.K252440EasyTeleMed (2.0.2)Ingeniars S.R.L.K250259TeleRehab Aermos Cardiopulmonary RehabilitationThe ScottCare Corporation K243837iBSMIorbit Digital Technologies Private Limited K242018UbiqVue™ 2A Multi-parameter System (UX2550)Lifesignals, Inc.K241101BioButton SystemBiointellisense, Inc.

Официальный источник

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