Haftungsausschluss: Diese Website bündelt öffentlich verfügbare Daten aus offiziellen Quellen wie FDA, ClinicalTrials.gov, PubMed und SEC EDGAR nur zur allgemeinen Information. Sie stellt keine medizinische Beratung, Diagnose, Behandlungsempfehlung oder Anlageberatung dar.

FDA 510(k)

BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System

K-Nummer: K160365 · 2016-09-28

AntragstellerInfopia Co, Ltd.
Entscheidungsdatum2016-09-28
ProduktcodeNBW
BeratungsausschussCH
EntscheidungSubstantially Equivalent

Produktübersicht

BLE Smart Blood Glucose Monitoring System, BLE Smart Professional Blood Glucose Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Infopia Co, Ltd.. It received FDA 510(k) clearance on 2016-09-28 under 510(k) number K160365. 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.

Häufig gestellte Fragen

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.

Zugehörige klinische Studien

Zugehörige Einträge werden automatisch anhand von Namen, Produktcodes oder anderen Metadaten abgeglichen. Eine Übereinstimmung begründet kein verifiziertes klinisches, wissenschaftliches, unternehmerisches oder regulatorisches Verhältnis; prüfen Sie die verlinkten offiziellen Quellen.

Verwandte Geräte (Code: NBW)

Zugehörige Einträge werden automatisch anhand von Namen, Produktcodes oder anderen Metadaten abgeglichen. Eine Übereinstimmung begründet kein verifiziertes klinisches, wissenschaftliches, unternehmerisches oder regulatorisches Verhältnis; prüfen Sie die verlinkten offiziellen Quellen.

Offizielle Quelle

In der FDA-Datenbank anzeigen →

Daten aus der FDA Open API. Für die aktuellsten und verbindlichen Informationen konsultieren Sie bitte stets den offiziellen Datensatz.

↑