ASCENSIA DEX 2 DIABETES CARE SYSTEM
K-Number: K023584 · 2002-11-20
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Device Summary
Frequently Asked Questions
What is the ASCENSIA DEX 2 DIABETES CARE SYSTEM?
ASCENSIA DEX 2 DIABETES CARE SYSTEM is a medical device that received FDA 510(k) clearance on 2002-11-20. The listed applicant is Bayer Corp.. The 510(k) number is K023584.
When did ASCENSIA DEX 2 DIABETES CARE SYSTEM receive FDA 510(k) clearance?
ASCENSIA DEX 2 DIABETES CARE SYSTEM received FDA 510(k) clearance on 2002-11-20, under 510(k) number K023584.
Who is the listed applicant for ASCENSIA DEX 2 DIABETES CARE SYSTEM?
The FDA 510(k) record lists Bayer Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASCENSIA DEX 2 DIABETES CARE SYSTEM?
The FDA product code for ASCENSIA DEX 2 DIABETES CARE 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 Bayer Corp. 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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