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FDA 510(k)

TSH RIA

K-Number: K833910 · 1983-11-22

ApplicantSyncor Intl. Corp.
Decision Date1983-11-22
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TSH RIA is the device name listed in this FDA 510(k) record. The listed applicant is Syncor Intl. Corp.. It received FDA 510(k) clearance on 1983-11-22 under 510(k) number K833910. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TSH RIA?

TSH RIA is a medical device that received FDA 510(k) clearance on 1983-11-22. The listed applicant is Syncor Intl. Corp.. The 510(k) number is K833910.

When did TSH RIA receive FDA 510(k) clearance?

TSH RIA received FDA 510(k) clearance on 1983-11-22, under 510(k) number K833910.

Who is the listed applicant for TSH RIA?

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

What is the FDA product code for TSH RIA?

The FDA product code for TSH RIA is ETD.

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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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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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