ABX MICROS CRP
K-Number: K002646 · 2000-10-26
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Device Summary
Frequently Asked Questions
What is the ABX MICROS CRP?
ABX MICROS CRP is a medical device that received FDA 510(k) clearance on 2000-10-26. The listed applicant is Abx Diagnostics. The 510(k) number is K002646.
When did ABX MICROS CRP receive FDA 510(k) clearance?
ABX MICROS CRP received FDA 510(k) clearance on 2000-10-26, under 510(k) number K002646.
Who is the listed applicant for ABX MICROS CRP?
The FDA 510(k) record lists Abx Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABX MICROS CRP?
The FDA product code for ABX MICROS CRP is GKZ.
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 Abx Diagnostics 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: GKZ)
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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