CYSTATIN C IMMUNOPARTICLES, CONTROL SET, CALIBRATOR
K-Number: K041627 · 2004-09-03
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement