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)

ACA HIGH DENSITY LIPOPROTEIN CHOLES.

K-Number: K792509 · 1980-01-11

Decision Date1980-01-11
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACA HIGH DENSITY LIPOPROTEIN CHOLES. is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1980-01-11 under 510(k) number K792509. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACA HIGH DENSITY LIPOPROTEIN CHOLES.?

ACA HIGH DENSITY LIPOPROTEIN CHOLES. is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K792509.

When did ACA HIGH DENSITY LIPOPROTEIN CHOLES. receive FDA 510(k) clearance?

ACA HIGH DENSITY LIPOPROTEIN CHOLES. received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792509.

Who is the listed applicant for ACA HIGH DENSITY LIPOPROTEIN CHOLES.?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACA HIGH DENSITY LIPOPROTEIN CHOLES.?

The FDA product code for ACA HIGH DENSITY LIPOPROTEIN CHOLES. is CHH.

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 E.I. Dupont DE Nemours & Co., 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 253 devices →

Related Devices (Code: CHH)

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.

↑