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FDA 510(k)

STANDARDS, HORMONE, THYROID STIMULATING

K-Number: K781071 · 1978-08-14

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

Device Summary

STANDARDS, HORMONE, THYROID STIMULATING 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 K781071. 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 STANDARDS, HORMONE, THYROID STIMULATING?

STANDARDS, HORMONE, THYROID STIMULATING 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 K781071.

When did STANDARDS, HORMONE, THYROID STIMULATING receive FDA 510(k) clearance?

STANDARDS, HORMONE, THYROID STIMULATING received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781071.

Who is the listed applicant for STANDARDS, HORMONE, THYROID STIMULATING?

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 STANDARDS, HORMONE, THYROID STIMULATING?

The FDA product code for STANDARDS, HORMONE, THYROID STIMULATING is JIT.

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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.

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Related Devices (Code: 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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