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FDA 510(k)

ACA THYRONINE UPTAKE (TU E) METHOD

K-Number: K885259 · 1989-02-17

ApplicantThe DU Pont Co.
Decision Date1989-02-17
Product CodeKHQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACA THYRONINE UPTAKE (TU E) METHOD is the device name listed in this FDA 510(k) record. The listed applicant is The DU Pont Co.. It received FDA 510(k) clearance on 1989-02-17 under 510(k) number K885259. The device is classified under product code KHQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACA THYRONINE UPTAKE (TU E) METHOD?

ACA THYRONINE UPTAKE (TU E) METHOD is a medical device that received FDA 510(k) clearance on 1989-02-17. The listed applicant is The DU Pont Co.. The 510(k) number is K885259.

When did ACA THYRONINE UPTAKE (TU E) METHOD receive FDA 510(k) clearance?

ACA THYRONINE UPTAKE (TU E) METHOD received FDA 510(k) clearance on 1989-02-17, under 510(k) number K885259.

Who is the listed applicant for ACA THYRONINE UPTAKE (TU E) METHOD?

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

What is the FDA product code for ACA THYRONINE UPTAKE (TU E) METHOD?

The FDA product code for ACA THYRONINE UPTAKE (TU E) METHOD is KHQ.

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Other records listing The DU Pont Co. 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.

K953475CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGINGK953477MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGINGK952891CRONEX LOW ABSORPTION CASSETTEK945125DUPONT ACA VANCOMYCIN (VANC) METHODK943704LIPASE CALIBRATORK900492LABELING CHANGE - VIASPAN(TM) (BELZER UW)

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Related Devices (Code: KHQ)

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.

K981375ACE T UPTAKE REAGENT TU CALIBRATORSSchiapparelli Biosystems, Inc.K980088T-UPTAKE MICROPLATE EIAMonobindK970539CHIRON DIAGNOSTICS ACS:180TU PChiron Diagnostics Corp.K964308VITROS IMMUNODIAGNOSTICS PRODUCTS T3 UPTAKE REAGENT PACK (GEM.1025) AND T3 UPTAKE CALIBRATORS (GEM.C025)Johnson & Johnson Clinical Diagnostics, Inc.K961488ELECSYS T-UPTAKE ASSAYBoehringer Mannheim Corp.K954807CEDIA T UPTAKE ASSAYBoehringer Mannheim 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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