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FDA 510(k)

1,25-DIHYDROXY VITAMIN D EIA

K-Number: K051110 · 2005-07-06

Decision Date2005-07-06
Product CodeMRG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

1,25-DIHYDROXY VITAMIN D EIA is the device name listed in this FDA 510(k) record. The listed applicant is Immunodiagnostic Systems , Ltd.. It received FDA 510(k) clearance on 2005-07-06 under 510(k) number K051110. 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 1,25-DIHYDROXY VITAMIN D EIA?

1,25-DIHYDROXY VITAMIN D EIA is a medical device that received FDA 510(k) clearance on 2005-07-06. The listed applicant is Immunodiagnostic Systems , Ltd.. The 510(k) number is K051110.

When did 1,25-DIHYDROXY VITAMIN D EIA receive FDA 510(k) clearance?

1,25-DIHYDROXY VITAMIN D EIA received FDA 510(k) clearance on 2005-07-06, under 510(k) number K051110.

Who is the listed applicant for 1,25-DIHYDROXY VITAMIN D EIA?

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

What is the FDA product code for 1,25-DIHYDROXY VITAMIN D EIA?

The FDA product code for 1,25-DIHYDROXY VITAMIN D EIA 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 Immunodiagnostic Systems , Ltd. 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 19 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.

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