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FDA 510(k)

DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD

K-Number: K870365 · 1987-08-19

Decision Date1987-08-19
Product CodeCIG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD is the device name listed in this FDA 510(k) record. The listed applicant is Trace Scientific , Ltd.. It received FDA 510(k) clearance on 1987-08-19 under 510(k) number K870365. 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 DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD?

DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD is a medical device that received FDA 510(k) clearance on 1987-08-19. The listed applicant is Trace Scientific , Ltd.. The 510(k) number is K870365.

When did DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD receive FDA 510(k) clearance?

DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD received FDA 510(k) clearance on 1987-08-19, under 510(k) number K870365.

Who is the listed applicant for DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD?

The FDA 510(k) record lists Trace Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD?

The FDA product code for DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD 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 Trace Scientific , Ltd. 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.

View all 55 devices →

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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