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FDA 510(k)

TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM

K-Number: K060120 · 2006-03-27

ApplicantTeco Diagnostics
Decision Date2006-03-27
Product CodeCDQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Teco Diagnostics. It received FDA 510(k) clearance on 2006-03-27 under 510(k) number K060120. The device is classified under product code CDQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM?

TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM is a medical device that received FDA 510(k) clearance on 2006-03-27. The listed applicant is Teco Diagnostics. The 510(k) number is K060120.

When did TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM receive FDA 510(k) clearance?

TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM received FDA 510(k) clearance on 2006-03-27, under 510(k) number K060120.

Who is the listed applicant for TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM?

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

What is the FDA product code for TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM?

The FDA product code for TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM is CDQ.

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Other records listing Teco 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.

K170118Scanostics UTI Check Application Test SystemK111206TECO DIAGNOSTICS SALIVA ALCOHOL TESTK100024TECO DIAGNOSTICS UTI DETECTION STRIPSK101673URITEK TC-101 URINE ANALYZER, URINE REAGENT STRIPS 10, MODELS TC-101, URS-10K073370TC MATRIX CLINICAL CHEMISTRY ANALYZERK072548CREATINE KINASE LIQUID REAGENT, MODEL C519-440

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Related Devices (Code: CDQ)

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.

K203771Urea Nitrogen2Abbott Ireland Diagnostics DivisionK110675EASYRA UREA NITROGEN AND CREATININE REAGENTSMedica Corp.K073295UREA/BUN, SCAL, NORTROL, ABTROLThermofisher Scientific OYK070146ABX PENTRA GLUCOSE HK CP, UREA CP, URIC ACID CPHoriba AbxK041051RAICHEM BUN RATE REAGENT (LIQUID)Hemagen Diagnostics, Inc.K024182PRECISION SYSTEMS ANALETTE CHEMISTRY ANALYZER STANBIO LABORATORY REAGENTSPrecision Systems, Inc.

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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