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FDA 510(k)

TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE

K-Number: K901122 · 1990-03-29

ApplicantTechnicon Instruments Corp.
Decision Date1990-03-29
Product CodeCFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE 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 1990-03-29 under 510(k) number K901122. The device is classified under product code CFR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE?

TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE is a medical device that received FDA 510(k) clearance on 1990-03-29. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K901122.

When did TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE receive FDA 510(k) clearance?

TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE received FDA 510(k) clearance on 1990-03-29, under 510(k) number K901122.

Who is the listed applicant for TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE?

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 CHEM 1 CLINICAL ANALYZER URINE GLUCOSE?

The FDA product code for TECHNICON CHEM 1 CLINICAL ANALYZER URINE GLUCOSE is CFR.

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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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