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FDA 510(k)

TEST, RIA, TSH QUANTIMUNE

K-Number: K760132 · 1976-07-20

ApplicantBio-Rad
Decision Date1976-07-20
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TEST, RIA, TSH QUANTIMUNE is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760132. The device is classified under product code JLW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEST, RIA, TSH QUANTIMUNE?

TEST, RIA, TSH QUANTIMUNE is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Bio-Rad. The 510(k) number is K760132.

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

TEST, RIA, TSH QUANTIMUNE received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760132.

Who is the listed applicant for TEST, RIA, TSH QUANTIMUNE?

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

What is the FDA product code for TEST, RIA, TSH QUANTIMUNE?

The FDA product code for TEST, RIA, TSH QUANTIMUNE is JLW.

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Related Devices (Code: JLW)

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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