VivaChek Ino Blood Glucose Monitoring System
K-Number: K160179 · 2017-04-21
Device Summary
Frequently Asked Questions
What is the VivaChek Ino Blood Glucose Monitoring System?
VivaChek Ino Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2017-04-21. The listed applicant is Vivachek Laboratories, Inc.. The 510(k) number is K160179.
When did VivaChek Ino Blood Glucose Monitoring System receive FDA 510(k) clearance?
VivaChek Ino Blood Glucose Monitoring System received FDA 510(k) clearance on 2017-04-21, under 510(k) number K160179.
Who is the listed applicant for VivaChek Ino Blood Glucose Monitoring System?
The FDA 510(k) record lists Vivachek Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VivaChek Ino Blood Glucose Monitoring System?
The FDA product code for VivaChek Ino Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.
Other records listing Vivachek Laboratories, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NBW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.