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FDA 510(k)

RABBIT ANTIBODY TO HUMAN T3

K-Number: K781284 · 1978-08-31

ApplicantPcl-Ria, Inc.
Decision Date1978-08-31
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RABBIT ANTIBODY TO HUMAN T3 is the device name listed in this FDA 510(k) record. The listed applicant is Pcl-Ria, Inc.. It received FDA 510(k) clearance on 1978-08-31 under 510(k) number K781284. The device is classified under product code CDP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RABBIT ANTIBODY TO HUMAN T3?

RABBIT ANTIBODY TO HUMAN T3 is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Pcl-Ria, Inc.. The 510(k) number is K781284.

When did RABBIT ANTIBODY TO HUMAN T3 receive FDA 510(k) clearance?

RABBIT ANTIBODY TO HUMAN T3 received FDA 510(k) clearance on 1978-08-31, under 510(k) number K781284.

Who is the listed applicant for RABBIT ANTIBODY TO HUMAN T3?

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

What is the FDA product code for RABBIT ANTIBODY TO HUMAN T3?

The FDA product code for RABBIT ANTIBODY TO HUMAN T3 is CDP.

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 Pcl-Ria, Inc. 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 29 devices →

Related Devices (Code: CDP)

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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