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FDA 510(k)

RADIAS 3RD GENERATION TSH IMMUNOASSAY

K-Number: K935119 · 1994-04-06

ApplicantBio-Rad
Decision Date1994-04-06
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RADIAS 3RD GENERATION TSH IMMUNOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1994-04-06 under 510(k) number K935119. 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 RADIAS 3RD GENERATION TSH IMMUNOASSAY?

RADIAS 3RD GENERATION TSH IMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1994-04-06. The listed applicant is Bio-Rad. The 510(k) number is K935119.

When did RADIAS 3RD GENERATION TSH IMMUNOASSAY receive FDA 510(k) clearance?

RADIAS 3RD GENERATION TSH IMMUNOASSAY received FDA 510(k) clearance on 1994-04-06, under 510(k) number K935119.

Who is the listed applicant for RADIAS 3RD GENERATION TSH IMMUNOASSAY?

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 RADIAS 3RD GENERATION TSH IMMUNOASSAY?

The FDA product code for RADIAS 3RD GENERATION TSH IMMUNOASSAY is JLW.

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 Bio-Rad 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: 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.

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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