ReliOn Premier BLU Blood Glucose Monitoring System
K-Number: K230625 · 2023-08-10
Device Summary
Frequently Asked Questions
What is the ReliOn Premier BLU Blood Glucose Monitoring System?
ReliOn Premier BLU Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2023-08-10. The listed applicant is I-Sens, Inc.. The 510(k) number is K230625.
When did ReliOn Premier BLU Blood Glucose Monitoring System receive FDA 510(k) clearance?
ReliOn Premier BLU Blood Glucose Monitoring System received FDA 510(k) clearance on 2023-08-10, under 510(k) number K230625.
Who is the listed applicant for ReliOn Premier BLU Blood Glucose Monitoring System?
The FDA 510(k) record lists I-Sens, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ReliOn Premier BLU Blood Glucose Monitoring System?
The FDA product code for ReliOn Premier BLU Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.
Other records listing I-Sens, 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.