Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MIO Blood Glucose Monitoring System

K-Number: K223722 · 2023-06-28

Decision Date2023-06-28
Product CodeNBW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MIO Blood Glucose Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Mio Labs, Inc.. It received FDA 510(k) clearance on 2023-06-28 under 510(k) number K223722. 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.

Frequently Asked Questions

What is the MIO Blood Glucose Monitoring System?

MIO Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2023-06-28. The listed applicant is Mio Labs, Inc.. The 510(k) number is K223722.

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

MIO Blood Glucose Monitoring System received FDA 510(k) clearance on 2023-06-28, under 510(k) number K223722.

Who is the listed applicant for MIO Blood Glucose Monitoring System?

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

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

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

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.