MCS ALBUMIN REAGENT
K-Number: K840291 · 1984-03-30
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Device Summary
Frequently Asked Questions
What is the MCS ALBUMIN REAGENT?
MCS ALBUMIN REAGENT is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Medilab Corp.. The 510(k) number is K840291.
When did MCS ALBUMIN REAGENT receive FDA 510(k) clearance?
MCS ALBUMIN REAGENT received FDA 510(k) clearance on 1984-03-30, under 510(k) number K840291.
Who is the listed applicant for MCS ALBUMIN REAGENT?
The FDA 510(k) record lists Medilab Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MCS ALBUMIN REAGENT?
The FDA product code for MCS ALBUMIN REAGENT is CIX.
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 Medilab Corp. 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: CIX)
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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