RDI LDL PRECIPITATION REAGENT
K-Number: K964063 · 1996-11-20
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Device Summary
Frequently Asked Questions
What is the RDI LDL PRECIPITATION REAGENT?
RDI LDL PRECIPITATION REAGENT is a medical device that received FDA 510(k) clearance on 1996-11-20. The listed applicant is Reference Diagnostics, Inc.. The 510(k) number is K964063.
When did RDI LDL PRECIPITATION REAGENT receive FDA 510(k) clearance?
RDI LDL PRECIPITATION REAGENT received FDA 510(k) clearance on 1996-11-20, under 510(k) number K964063.
Who is the listed applicant for RDI LDL PRECIPITATION REAGENT?
The FDA 510(k) record lists Reference Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RDI LDL PRECIPITATION REAGENT?
The FDA product code for RDI LDL PRECIPITATION REAGENT is MRR.
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 Reference Diagnostics, 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.
Related Devices (Code: MRR)
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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