OLYMPUS DIRECT BILIRUBIN
K-Number: K897175 · 1990-03-15
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Device Summary
Frequently Asked Questions
What is the OLYMPUS DIRECT BILIRUBIN?
OLYMPUS DIRECT BILIRUBIN is a medical device that received FDA 510(k) clearance on 1990-03-15. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K897175.
When did OLYMPUS DIRECT BILIRUBIN receive FDA 510(k) clearance?
OLYMPUS DIRECT BILIRUBIN received FDA 510(k) clearance on 1990-03-15, under 510(k) number K897175.
Who is the listed applicant for OLYMPUS DIRECT BILIRUBIN?
The FDA 510(k) record lists Em Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OLYMPUS DIRECT BILIRUBIN?
The FDA product code for OLYMPUS DIRECT BILIRUBIN is CIG.
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 Em Diagnostic Systems, 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: CIG)
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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