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FDA 510(k)

TECHNICON RA-XT SYSTEM WITH ANALYTES

K-Number: K862561 · 1986-10-20

ApplicantTechnicon Instruments Corp.
Decision Date1986-10-20
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON RA-XT SYSTEM WITH ANALYTES is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1986-10-20 under 510(k) number K862561. 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-XT SYSTEM WITH ANALYTES?

TECHNICON RA-XT SYSTEM WITH ANALYTES is a medical device that received FDA 510(k) clearance on 1986-10-20. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K862561.

When did TECHNICON RA-XT SYSTEM WITH ANALYTES receive FDA 510(k) clearance?

TECHNICON RA-XT SYSTEM WITH ANALYTES received FDA 510(k) clearance on 1986-10-20, under 510(k) number K862561.

Who is the listed applicant for TECHNICON RA-XT SYSTEM WITH ANALYTES?

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

What is the FDA product code for TECHNICON RA-XT SYSTEM WITH ANALYTES?

The FDA product code for TECHNICON RA-XT SYSTEM WITH ANALYTES is JJC.

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Other records listing Technicon Instruments Corp. as applicant

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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

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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