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FDA 510(k)

RIA SYSTEM FOR HUMAN F-S HORMONE

K-Number: K780870 · 1978-06-22

Decision Date1978-06-22
Product CodeCGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA SYSTEM FOR HUMAN F-S HORMONE is the device name listed in this FDA 510(k) record. The listed applicant is Calbiochem-Behring Corp.. It received FDA 510(k) clearance on 1978-06-22 under 510(k) number K780870. The device is classified under product code CGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA SYSTEM FOR HUMAN F-S HORMONE?

RIA SYSTEM FOR HUMAN F-S HORMONE is a medical device that received FDA 510(k) clearance on 1978-06-22. The listed applicant is Calbiochem-Behring Corp.. The 510(k) number is K780870.

When did RIA SYSTEM FOR HUMAN F-S HORMONE receive FDA 510(k) clearance?

RIA SYSTEM FOR HUMAN F-S HORMONE received FDA 510(k) clearance on 1978-06-22, under 510(k) number K780870.

Who is the listed applicant for RIA SYSTEM FOR HUMAN F-S HORMONE?

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

What is the FDA product code for RIA SYSTEM FOR HUMAN F-S HORMONE?

The FDA product code for RIA SYSTEM FOR HUMAN F-S HORMONE is CGJ.

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 Calbiochem-Behring 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 41 devices →

Related Devices (Code: CGJ)

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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