COBAS READY TOTAL BILIRUBIN REAGENT
K-Number: K896232 · 1990-02-27
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Device Summary
Frequently Asked Questions
What is the COBAS READY TOTAL BILIRUBIN REAGENT?
COBAS READY TOTAL BILIRUBIN REAGENT is a medical device that received FDA 510(k) clearance on 1990-02-27. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K896232.
When did COBAS READY TOTAL BILIRUBIN REAGENT receive FDA 510(k) clearance?
COBAS READY TOTAL BILIRUBIN REAGENT received FDA 510(k) clearance on 1990-02-27, under 510(k) number K896232.
Who is the listed applicant for COBAS READY TOTAL BILIRUBIN REAGENT?
The FDA 510(k) record lists Roche Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COBAS READY TOTAL BILIRUBIN REAGENT?
The FDA product code for COBAS READY TOTAL BILIRUBIN REAGENT 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 Roche 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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