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FDA 510(k)

RHEUMADX LATEX AGGLUTINATION RHEUMATOID

K-Number: K843896 · 1984-10-25

ApplicantDiagnostic Products Corp.
Decision Date1984-10-25
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RHEUMADX LATEX AGGLUTINATION RHEUMATOID is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1984-10-25 under 510(k) number K843896. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHEUMADX LATEX AGGLUTINATION RHEUMATOID?

RHEUMADX LATEX AGGLUTINATION RHEUMATOID is a medical device that received FDA 510(k) clearance on 1984-10-25. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K843896.

When did RHEUMADX LATEX AGGLUTINATION RHEUMATOID receive FDA 510(k) clearance?

RHEUMADX LATEX AGGLUTINATION RHEUMATOID received FDA 510(k) clearance on 1984-10-25, under 510(k) number K843896.

Who is the listed applicant for RHEUMADX LATEX AGGLUTINATION RHEUMATOID?

The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RHEUMADX LATEX AGGLUTINATION RHEUMATOID?

The FDA product code for RHEUMADX LATEX AGGLUTINATION RHEUMATOID is DHR.

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Other records listing Diagnostic Products Corp. as applicant

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Related Devices (Code: DHR)

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.

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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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