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FDA 510(k)

EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G

K-Number: K062555 · 2006-12-27

Decision Date2006-12-27
Product CodeNBW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G is the device name listed in this FDA 510(k) record. The listed applicant is Visgeneer, Inc.. It received FDA 510(k) clearance on 2006-12-27 under 510(k) number K062555. 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 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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