NICHOLS ADVANTAGE CORTISOL
K-Number: K042689 · 2004-12-09
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Device Summary
Frequently Asked Questions
What is the NICHOLS ADVANTAGE CORTISOL?
NICHOLS ADVANTAGE CORTISOL is a medical device that received FDA 510(k) clearance on 2004-12-09. The listed applicant is Nichols Institute Diagnostics. The 510(k) number is K042689.
When did NICHOLS ADVANTAGE CORTISOL receive FDA 510(k) clearance?
NICHOLS ADVANTAGE CORTISOL received FDA 510(k) clearance on 2004-12-09, under 510(k) number K042689.
Who is the listed applicant for NICHOLS ADVANTAGE CORTISOL?
The FDA 510(k) record lists Nichols Institute Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NICHOLS ADVANTAGE CORTISOL?
The FDA product code for NICHOLS ADVANTAGE CORTISOL is CGR.
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 Nichols Institute 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: CGR)
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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