FDA 510(k)

Hach CM130 Chlorine Monitoring System

Номер K: K162471 · 2017-03-30

ЗаявительHach Company

Дата решения2017-03-30

Код продуктаPSX

Консультативный комитетGU

РешениеSubstantially Equivalent

Описание устройства

Hach CM130 Chlorine Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Hach Company. It received FDA 510(k) clearance on 2017-03-30 under 510(k) number K162471. The device is classified under product code PSX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the Hach CM130 Chlorine Monitoring System?

Hach CM130 Chlorine Monitoring System is a medical device that received FDA 510(k) clearance on 2017-03-30. The listed applicant is Hach Company. The 510(k) number is K162471.

When did Hach CM130 Chlorine Monitoring System receive FDA 510(k) clearance?

Hach CM130 Chlorine Monitoring System received FDA 510(k) clearance on 2017-03-30, under 510(k) number K162471.

Who is the listed applicant for Hach CM130 Chlorine Monitoring System?

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

What is the FDA product code for Hach CM130 Chlorine Monitoring System?

The FDA product code for Hach CM130 Chlorine Monitoring System is PSX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Официальный источник

Посмотреть в базе данных FDA →

Данные получены из открытого API FDA. Для получения наиболее актуальной и авторитетной информации всегда обращайтесь к официальным записям.