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FDA 510(k)

THEOPHYLLINE RIASSAY

K-Number: K792062 · 1980-02-25

ApplicantRia Diagnostics
Decision Date1980-02-25
Product CodeLCA
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

THEOPHYLLINE RIASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Ria Diagnostics. It received FDA 510(k) clearance on 1980-02-25 under 510(k) number K792062. The device is classified under product code LCA. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THEOPHYLLINE RIASSAY?

THEOPHYLLINE RIASSAY is a medical device that received FDA 510(k) clearance on 1980-02-25. The listed applicant is Ria Diagnostics. The 510(k) number is K792062.

When did THEOPHYLLINE RIASSAY receive FDA 510(k) clearance?

THEOPHYLLINE RIASSAY received FDA 510(k) clearance on 1980-02-25, under 510(k) number K792062.

Who is the listed applicant for THEOPHYLLINE RIASSAY?

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

What is the FDA product code for THEOPHYLLINE RIASSAY?

The FDA product code for THEOPHYLLINE RIASSAY is LCA.

Related Clinical Trials

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Other records listing Ria Diagnostics 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.

K855033T-3 UPTAKE/RIASSAYK854798T-4 RIASSAYK852537T-3 RIASSAYK810296DIGOXIN RIA ASSAYK801691TSH RIASSAYK780012ANTITHROMBIN III RIA

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Related Devices (Code: LCA)

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.

K880291THEOPHYLLINE TEST KIT REF. #A874799Photec Diagnostics, Inc.K833789PHASE II THEOPHYLLINE RADIOIMMUNOASSAYMedical & Scientific Designs, Inc.K821862QUANTICOAT 125 I-THEOPHYLLINE RADIOIMM.Kallestad Laboratories, Inc.K821347BIO-MAG THEOPHYLLINE (125I) RADIOIMMUN.Bioclinical Corp.

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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