Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MODIFIED ENZYMATIC BUN REAGENT

K-Number: K872484 · 1987-08-19

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

Device Summary

MODIFIED ENZYMATIC BUN REAGENT 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 K872484. The device is classified under product code CDQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED ENZYMATIC BUN REAGENT?

MODIFIED ENZYMATIC BUN REAGENT 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 K872484.

When did MODIFIED ENZYMATIC BUN REAGENT receive FDA 510(k) clearance?

MODIFIED ENZYMATIC BUN REAGENT received FDA 510(k) clearance on 1987-08-19, under 510(k) number K872484.

Who is the listed applicant for MODIFIED ENZYMATIC BUN REAGENT?

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 MODIFIED ENZYMATIC BUN REAGENT?

The FDA product code for MODIFIED ENZYMATIC BUN REAGENT is CDQ.

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: CDQ)

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.

↑