ELEMENT BLOOD GLUCOSE TEST SYSTEM
K-Number: K060793 · 2006-07-25
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Device Summary
Frequently Asked Questions
What is the ELEMENT BLOOD GLUCOSE TEST SYSTEM?
ELEMENT BLOOD GLUCOSE TEST SYSTEM is a medical device that received FDA 510(k) clearance on 2006-07-25. The listed applicant is Home Diagnostics, Inc.. The 510(k) number is K060793.
When did ELEMENT BLOOD GLUCOSE TEST SYSTEM receive FDA 510(k) clearance?
ELEMENT BLOOD GLUCOSE TEST SYSTEM received FDA 510(k) clearance on 2006-07-25, under 510(k) number K060793.
Who is the listed applicant for ELEMENT BLOOD GLUCOSE TEST SYSTEM?
The FDA 510(k) record lists Home Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELEMENT BLOOD GLUCOSE TEST SYSTEM?
The FDA product code for ELEMENT BLOOD GLUCOSE TEST 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 Home Diagnostics, 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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