GAMMA-B 1,25-DIHYDROXY VITAMIN D
K-Number: K042519 · 2004-12-01
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Device Summary
Frequently Asked Questions
What is the GAMMA-B 1,25-DIHYDROXY VITAMIN D?
GAMMA-B 1,25-DIHYDROXY VITAMIN D is a medical device that received FDA 510(k) clearance on 2004-12-01. The listed applicant is Immunodiagnostic Systems , Ltd.. The 510(k) number is K042519.
When did GAMMA-B 1,25-DIHYDROXY VITAMIN D receive FDA 510(k) clearance?
GAMMA-B 1,25-DIHYDROXY VITAMIN D received FDA 510(k) clearance on 2004-12-01, under 510(k) number K042519.
Who is the listed applicant for GAMMA-B 1,25-DIHYDROXY VITAMIN D?
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 GAMMA-B 1,25-DIHYDROXY VITAMIN D?
The FDA product code for GAMMA-B 1,25-DIHYDROXY 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 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.
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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