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FDA 510(k)

VISTA FREE THYROXINE ASSAY

K-Number: K923572 · 1992-11-16

ApplicantSyva Co.
Decision Date1992-11-16
Product CodeCEC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VISTA FREE THYROXINE ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1992-11-16 under 510(k) number K923572. The device is classified under product code CEC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTA FREE THYROXINE ASSAY?

VISTA FREE THYROXINE ASSAY is a medical device that received FDA 510(k) clearance on 1992-11-16. The listed applicant is Syva Co.. The 510(k) number is K923572.

When did VISTA FREE THYROXINE ASSAY receive FDA 510(k) clearance?

VISTA FREE THYROXINE ASSAY received FDA 510(k) clearance on 1992-11-16, under 510(k) number K923572.

Who is the listed applicant for VISTA FREE THYROXINE ASSAY?

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

What is the FDA product code for VISTA FREE THYROXINE ASSAY?

The FDA product code for VISTA FREE THYROXINE ASSAY is CEC.

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Other records listing Syva Co. as applicant

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Related Devices (Code: CEC)

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.

K240273Access Free T4Beckman Coulter, Inc.K220456Elecsys FT4 IVRoche DiagnosticsK182423MAGLUMI 2000 FT4Shenzhen New Industries Biomedical Engineering Co., Ltd.K181233Elecsys FT4 IIIRoche DiagnosticsK173122Abbott Architect Free T4Abbott LaboratoriesK152422FREND™ Free T4 Test SystemNanoentek USA, Inc.

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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