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FDA 510(k)

CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR

K-Number: K041627 · 2004-09-03

ApplicantDako A/S
Decision Date2004-09-03
Product CodeNDY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Dako A/S. It received FDA 510(k) clearance on 2004-09-03 under 510(k) number K041627. The device is classified under product code NDY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR?

CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR is a medical device that received FDA 510(k) clearance on 2004-09-03. The listed applicant is Dako A/S. The 510(k) number is K041627.

When did CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR receive FDA 510(k) clearance?

CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR received FDA 510(k) clearance on 2004-09-03, under 510(k) number K041627.

Who is the listed applicant for CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR?

The FDA 510(k) record lists Dako A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR?

The FDA product code for CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR is NDY.

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 Dako A/S 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: NDY)

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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