FDA 510(k)

Finetest Lite Blood Glucose Monitoring System

Número K: K203562 · 2021-07-13

Data da decisão2021-07-13

Código do produtoNBW

Comité consultivoCH

DecisãoSubstantially Equivalent

Resumo do dispositivo

Finetest Lite Blood Glucose Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Osang Healthcare Co. , Ltd.. It received FDA 510(k) clearance on 2021-07-13 under 510(k) number K203562. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Finetest Lite Blood Glucose Monitoring System?

Finetest Lite Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2021-07-13. The listed applicant is Osang Healthcare Co. , Ltd.. The 510(k) number is K203562.

When did Finetest Lite Blood Glucose Monitoring System receive FDA 510(k) clearance?

Finetest Lite Blood Glucose Monitoring System received FDA 510(k) clearance on 2021-07-13, under 510(k) number K203562.

Who is the listed applicant for Finetest Lite Blood Glucose Monitoring System?

The FDA 510(k) record lists Osang Healthcare Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Finetest Lite Blood Glucose Monitoring System?

The FDA product code for Finetest Lite Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.

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Outros registros que listam Osang Healthcare Co. , Ltd. como candidato(a)

K201396Finetest Lite Smart Blood Glucose Monitoring System K182286Oh'Care Lite Smart Blood Glucose Monitoring System

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