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FDA 510(k)

ROCHE REAGENT FOR TOTAL BILIRUBIN

K-Number: K910591 · 1991-04-24

Decision Date1991-04-24
Product CodeCIG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ROCHE REAGENT FOR TOTAL BILIRUBIN is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1991-04-24 under 510(k) number K910591. The device is classified under product code CIG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROCHE REAGENT FOR TOTAL BILIRUBIN?

ROCHE REAGENT FOR TOTAL BILIRUBIN is a medical device that received FDA 510(k) clearance on 1991-04-24. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K910591.

When did ROCHE REAGENT FOR TOTAL BILIRUBIN receive FDA 510(k) clearance?

ROCHE REAGENT FOR TOTAL BILIRUBIN received FDA 510(k) clearance on 1991-04-24, under 510(k) number K910591.

Who is the listed applicant for ROCHE REAGENT FOR TOTAL BILIRUBIN?

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 ROCHE REAGENT FOR TOTAL BILIRUBIN?

The FDA product code for ROCHE REAGENT FOR TOTAL 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 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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