BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System
Номер K: K160365 · 2016-09-28
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Описание устройства
Часто задаваемые вопросы
What is the BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System?
BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2016-09-28. The listed applicant is Infopia Co, Ltd.. The 510(k) number is K160365.
When did BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System receive FDA 510(k) clearance?
BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System received FDA 510(k) clearance on 2016-09-28, under 510(k) number K160365.
Who is the listed applicant for BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System?
The FDA 510(k) record lists Infopia Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System?
The FDA product code for BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.
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.
Связанные устройства (Код: NBW)
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.
Официальный источник
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