OLYMPUS ALBUMIN REAGENT
K-Number: K924368 · 1993-02-08
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Device Summary
Frequently Asked Questions
What is the OLYMPUS ALBUMIN REAGENT?
OLYMPUS ALBUMIN REAGENT is a medical device that received FDA 510(k) clearance on 1993-02-08. The listed applicant is Olympus Corp.. The 510(k) number is K924368.
When did OLYMPUS ALBUMIN REAGENT receive FDA 510(k) clearance?
OLYMPUS ALBUMIN REAGENT received FDA 510(k) clearance on 1993-02-08, under 510(k) number K924368.
Who is the listed applicant for OLYMPUS ALBUMIN REAGENT?
The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OLYMPUS ALBUMIN REAGENT?
The FDA product code for OLYMPUS 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 Olympus 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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