FDA 510(k)

GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System

K-Nummer: K193340 · 2020-09-11

Entscheidungsdatum2020-09-11

ProduktcodeNBW

BeratungsausschussCH

EntscheidungSubstantially Equivalent

Produktübersicht

GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Microtech Medical, Inc.. It received FDA 510(k) clearance on 2020-09-11 under 510(k) number K193340. 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 GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System?

GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2020-09-11. The listed applicant is Microtech Medical, Inc.. The 510(k) number is K193340.

When did GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System receive FDA 510(k) clearance?

GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System received FDA 510(k) clearance on 2020-09-11, under 510(k) number K193340.

Who is the listed applicant for GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System?

The FDA 510(k) record lists Microtech Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GoChek Blood Glucose Monitoring System, GoChek Connect Blood Glucose Monitoring System?

The FDA product code for GoChek Blood Glucose Monitoring System, GoChek Connect 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.

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

Verwandte Geräte (Code: NBW)

K260545CONTOUR® PLUS BLUE Blood Glucose Monitoring System; CONTOUR® NEXT GEN Blood Glucose Monitoring System; CONTOUR® NEXT ONE Blood Glucose Monitoring SystemAscensia Diabetes Care K262116TRUE METRIX Self Monitoring Blood Glucose SystemTrividia Health, Inc.K250085On Call® Sure GK Blood Glucose & Ketone Monitoring System; On Call® Sure Sync GK Blood Glucose & Ketone Monitoring SystemACON Laboratories, Inc.K243060TeleRPM Gen2 Blood Glucose Monitoring SystemGuangdong Transtek Medical Electronics Co., Ltd.K240637RIGHTEST Blood Glucose Monitoring System Max TelBionime Corporation K240640Sejoy Blood Glucose Monitoring System; Sejoy Advance Link Blood Glucose Monitoring SystemSejoy Biomedical Co., Ltd.

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.