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FDA 510(k)

1,25-DIHYDROXYVITAMIN D125I RIA

K-Number: K014030 · 2002-03-26

ApplicantDiaSorin, Inc.
Decision Date2002-03-26
Product CodeMRG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

1,25-DIHYDROXYVITAMIN D125I RIA is the device name listed in this FDA 510(k) record. The listed applicant is DiaSorin, Inc.. It received FDA 510(k) clearance on 2002-03-26 under 510(k) number K014030. 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-DIHYDROXYVITAMIN D125I RIA?

1,25-DIHYDROXYVITAMIN D125I RIA is a medical device that received FDA 510(k) clearance on 2002-03-26. The listed applicant is DiaSorin, Inc.. The 510(k) number is K014030.

When did 1,25-DIHYDROXYVITAMIN D125I RIA receive FDA 510(k) clearance?

1,25-DIHYDROXYVITAMIN D125I RIA received FDA 510(k) clearance on 2002-03-26, under 510(k) number K014030.

Who is the listed applicant for 1,25-DIHYDROXYVITAMIN D125I RIA?

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 1,25-DIHYDROXYVITAMIN D125I RIA?

The FDA product code for 1,25-DIHYDROXYVITAMIN D125I RIA is MRG.

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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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