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FDA 510(k)

TIA-IGA REAGENT & CALIBRATOR SETS

K-Number: K831102 · 1983-04-27

Decision Date1983-04-27
Product CodeCZP
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TIA-IGA REAGENT & CALIBRATOR SETS is the device name listed in this FDA 510(k) record. The listed applicant is Worthington Diagnostic Systems. It received FDA 510(k) clearance on 1983-04-27 under 510(k) number K831102. The device is classified under product code CZP. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIA-IGA REAGENT & CALIBRATOR SETS?

TIA-IGA REAGENT & CALIBRATOR SETS is a medical device that received FDA 510(k) clearance on 1983-04-27. The listed applicant is Worthington Diagnostic Systems. The 510(k) number is K831102.

When did TIA-IGA REAGENT & CALIBRATOR SETS receive FDA 510(k) clearance?

TIA-IGA REAGENT & CALIBRATOR SETS received FDA 510(k) clearance on 1983-04-27, under 510(k) number K831102.

Who is the listed applicant for TIA-IGA REAGENT & CALIBRATOR SETS?

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

What is the FDA product code for TIA-IGA REAGENT & CALIBRATOR SETS?

The FDA product code for TIA-IGA REAGENT & CALIBRATOR SETS is CZP.

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 Worthington Diagnostic Systems 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.

View all 19 devices →

Related Devices (Code: CZP)

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

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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