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)

GLUCOSE OXIDASE REAGENT

K-Number: K800589 · 1980-04-04

Decision Date1980-04-04
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOSE OXIDASE REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Scientific Industries, Inc.. It received FDA 510(k) clearance on 1980-04-04 under 510(k) number K800589. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLUCOSE OXIDASE REAGENT?

GLUCOSE OXIDASE REAGENT is a medical device that received FDA 510(k) clearance on 1980-04-04. The listed applicant is Nobel Scientific Industries, Inc.. The 510(k) number is K800589.

When did GLUCOSE OXIDASE REAGENT receive FDA 510(k) clearance?

GLUCOSE OXIDASE REAGENT received FDA 510(k) clearance on 1980-04-04, under 510(k) number K800589.

Who is the listed applicant for GLUCOSE OXIDASE REAGENT?

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

What is the FDA product code for GLUCOSE OXIDASE REAGENT?

The FDA product code for GLUCOSE OXIDASE REAGENT is CGA.

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 Nobel Scientific Industries, 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.

View all 23 devices →

Related Devices (Code: CGA)

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.

↑