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FDA 510(k)

FIAX 420 DILUTOR

K-Number: K843621 · 1984-09-28

ApplicantIntl. Diagnostic Technology
Decision Date1984-09-28
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FIAX 420 DILUTOR is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Diagnostic Technology. It received FDA 510(k) clearance on 1984-09-28 under 510(k) number K843621. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIAX 420 DILUTOR?

FIAX 420 DILUTOR is a medical device that received FDA 510(k) clearance on 1984-09-28. The listed applicant is Intl. Diagnostic Technology. The 510(k) number is K843621.

When did FIAX 420 DILUTOR receive FDA 510(k) clearance?

FIAX 420 DILUTOR received FDA 510(k) clearance on 1984-09-28, under 510(k) number K843621.

Who is the listed applicant for FIAX 420 DILUTOR?

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

What is the FDA product code for FIAX 420 DILUTOR?

The FDA product code for FIAX 420 DILUTOR is JQW.

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Other records listing Intl. Diagnostic Technology 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.

K850591FIAX TOXO-M ANTIBODIES TEST KITK843570FIAX HAPTOGLOBIN TEST KITK843356FIAX 100 FLUOROMETERK842749FIAX TOTAL IGE TEST KITK842071FIAX TRANSFERRIN TEST KITK841174RUBELLA ANTIBODY FLUOROIMMUNOASSAY

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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