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FDA 510(k)

ADP ANA IFA TEST

K-Number: K842183 · 1984-06-22

Decision Date1984-06-22
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ADP ANA IFA TEST is the device name listed in this FDA 510(k) record. The listed applicant is Apple Diagnostic Products. It received FDA 510(k) clearance on 1984-06-22 under 510(k) number K842183. 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 ADP ANA IFA TEST?

ADP ANA IFA TEST is a medical device that received FDA 510(k) clearance on 1984-06-22. The listed applicant is Apple Diagnostic Products. The 510(k) number is K842183.

When did ADP ANA IFA TEST receive FDA 510(k) clearance?

ADP ANA IFA TEST received FDA 510(k) clearance on 1984-06-22, under 510(k) number K842183.

Who is the listed applicant for ADP ANA IFA TEST?

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

What is the FDA product code for ADP ANA IFA TEST?

The FDA product code for ADP ANA IFA TEST is DHN.

Other records listing Apple Diagnostic Products 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 7 devices →

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.

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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