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FDA 510(k)

CHOLESTEROL REAGENT SUBSTRATE SET

K-Number: K781970 · 1979-01-03

Decision Date1979-01-03
Product CodeJHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHOLESTEROL REAGENT SUBSTRATE SET is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1979-01-03 under 510(k) number K781970. The device is classified under product code JHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHOLESTEROL REAGENT SUBSTRATE SET?

CHOLESTEROL REAGENT SUBSTRATE SET is a medical device that received FDA 510(k) clearance on 1979-01-03. The listed applicant is Corning Medical & Scientific. The 510(k) number is K781970.

When did CHOLESTEROL REAGENT SUBSTRATE SET receive FDA 510(k) clearance?

CHOLESTEROL REAGENT SUBSTRATE SET received FDA 510(k) clearance on 1979-01-03, under 510(k) number K781970.

Who is the listed applicant for CHOLESTEROL REAGENT SUBSTRATE SET?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHOLESTEROL REAGENT SUBSTRATE SET?

The FDA product code for CHOLESTEROL REAGENT SUBSTRATE SET is JHO.

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 Corning Medical & Scientific 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 111 devices →

Related Devices (Code: JHO)

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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