DIRECT BILIRUBIN REAGENT - ACID DIAZO METHOD
K-Number: K870365 · 1987-08-19
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Device Summary
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.
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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