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FDA 510(k)

T3 STANDARDS IN HUMAN SERUM

K-Number: K781069 · 1978-08-14

ApplicantPcl-Ria, Inc.
Decision Date1978-08-14
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

T3 STANDARDS IN HUMAN SERUM 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 1978-08-14 under 510(k) number K781069. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T3 STANDARDS IN HUMAN SERUM?

T3 STANDARDS IN HUMAN SERUM is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Pcl-Ria, Inc.. The 510(k) number is K781069.

When did T3 STANDARDS IN HUMAN SERUM receive FDA 510(k) clearance?

T3 STANDARDS IN HUMAN SERUM received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781069.

Who is the listed applicant for T3 STANDARDS IN HUMAN SERUM?

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 T3 STANDARDS IN HUMAN SERUM?

The FDA product code for T3 STANDARDS IN HUMAN SERUM is JIT.

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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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