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FDA 510(k)

GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY

K-Number: K842079 · 1984-06-26

Decision Date1984-06-26
Product CodeCGC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Immuno Nuclear Corp.. It received FDA 510(k) clearance on 1984-06-26 under 510(k) number K842079. The device is classified under product code CGC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY?

GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1984-06-26. The listed applicant is Immuno Nuclear Corp.. The 510(k) number is K842079.

When did GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY receive FDA 510(k) clearance?

GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY received FDA 510(k) clearance on 1984-06-26, under 510(k) number K842079.

Who is the listed applicant for GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY?

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

What is the FDA product code for GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY?

The FDA product code for GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY is CGC.

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 Immuno Nuclear Corp. 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 30 devices →

Related Devices (Code: CGC)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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