EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G
K-Number: K062555 · 2006-12-27
Advertisement
Device Summary
Frequently Asked Questions
What is the EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G?
EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G is a medical device that received FDA 510(k) clearance on 2006-12-27. The listed applicant is Visgeneer, Inc.. The 510(k) number is K062555.
When did EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G receive FDA 510(k) clearance?
EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G received FDA 510(k) clearance on 2006-12-27, under 510(k) number K062555.
Who is the listed applicant for EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G?
The FDA 510(k) record lists Visgeneer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G?
The FDA product code for EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G is NBW. This falls under the OB/GYN category.
Related Clinical Trials
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.
Other records listing Visgeneer, 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.
Advertisement