EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM
K-Number: K091765 · 2010-01-19
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Device Summary
Frequently Asked Questions
What is the EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM?
EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2010-01-19. The listed applicant is Visgeneer, Inc.. The 510(k) number is K091765.
When did EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM receive FDA 510(k) clearance?
EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM received FDA 510(k) clearance on 2010-01-19, under 510(k) number K091765.
Who is the listed applicant for EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM?
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 EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM?
The FDA product code for EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM 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.
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