Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIAISON 25 OH VITAMIN D

K-Number: K032844 · 2004-02-12

Decision Date2004-02-12
Product CodeMRG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIAISON 25 OH VITAMIN D is the device name listed in this FDA 510(k) record. The listed applicant is DiaSorin, Inc.. It received FDA 510(k) clearance on 2004-02-12 under 510(k) number K032844. The device is classified under product code MRG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIAISON 25 OH VITAMIN D?

LIAISON 25 OH VITAMIN D is a medical device that received FDA 510(k) clearance on 2004-02-12. The listed applicant is DiaSorin, Inc.. The 510(k) number is K032844.

When did LIAISON 25 OH VITAMIN D receive FDA 510(k) clearance?

LIAISON 25 OH VITAMIN D received FDA 510(k) clearance on 2004-02-12, under 510(k) number K032844.

Who is the listed applicant for LIAISON 25 OH VITAMIN D?

The FDA 510(k) record lists DiaSorin, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIAISON 25 OH VITAMIN D?

The FDA product code for LIAISON 25 OH VITAMIN D is MRG.

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 DiaSorin, Inc. 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.

View all 66 devices →

Related Devices (Code: MRG)

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.

↑