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FDA 510(k)

ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP

K-Number: K760209 · 1976-07-26

ApplicantZeus Scientific, Inc.
Decision Date1976-07-26
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP is the device name listed in this FDA 510(k) record. The listed applicant is Zeus Scientific, Inc.. It received FDA 510(k) clearance on 1976-07-26 under 510(k) number K760209. The device is classified under product code DHN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP?

ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP is a medical device that received FDA 510(k) clearance on 1976-07-26. The listed applicant is Zeus Scientific, Inc.. The 510(k) number is K760209.

When did ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP receive FDA 510(k) clearance?

ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP received FDA 510(k) clearance on 1976-07-26, under 510(k) number K760209.

Who is the listed applicant for ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP?

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

What is the FDA product code for ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP?

The FDA product code for ACID, NATIVE-DEOXYRIBONUCLEIC, IVDP is DHN.

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Other records listing Zeus Scientific, Inc. as applicant

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Related Devices (Code: DHN)

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.

K201956Zeus IFA ANA HEp-2 Test System, Zeus dIFineZeus Scientific, Inc.K172745ImmuGlo HEp-2 Elite IFAImmco Diagnostics, Inc.K153117AESKUSLIDES ANA HEp-2-Gamma, HELIOS FULLY AUTOMATED IFA SYSTEMAesku Systems GmbH&Co.KgK160265Image Navigator by Immuno ConceptsImmuno Concepts, N.A. , Ltd.K120889AESKUSLIDES ANA HEP-2Aesku DiagnosticsK070763EUROIMMUN ANA IFA: HEP-20-10Euroimmun Us, LLC

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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