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FDA 510(k)

TECHNICON RA 1000 SYSTEM

K-Number: K813077 · 1981-11-16

ApplicantTechnicon Corp.
Decision Date1981-11-16
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON RA 1000 SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Corp.. It received FDA 510(k) clearance on 1981-11-16 under 510(k) number K813077. The device is classified under product code JJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON RA 1000 SYSTEM?

TECHNICON RA 1000 SYSTEM is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Technicon Corp.. The 510(k) number is K813077.

When did TECHNICON RA 1000 SYSTEM receive FDA 510(k) clearance?

TECHNICON RA 1000 SYSTEM received FDA 510(k) clearance on 1981-11-16, under 510(k) number K813077.

Who is the listed applicant for TECHNICON RA 1000 SYSTEM?

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

What is the FDA product code for TECHNICON RA 1000 SYSTEM?

The FDA product code for TECHNICON RA 1000 SYSTEM is JJC.

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.

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Other records listing Technicon Corp. 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.

K791323TECHNION ELECTRONIC FEVER THERMOMETER

Related Devices (Code: JJC)

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.

K945915AVL OMNI ANALYZERAvl Scientific Corp.K945584NOVA 16 ANALYZERNova Biomedical Corp.K943376OPERA SYSTEMMiles, Inc.K901410TECHNICON RA-2000(TM) SYSTEMTechnicon Instruments Corp.K901141PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZXBaxter Healthcare CorpK890332RFA/2 RAPID FLOW ANALYZER W/COMPUTERAlpkem Corp.

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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