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FDA 510(k)

ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA.

K-Number: K884168 · 1988-11-29

ApplicantThe DU Pont Co.
Decision Date1988-11-29
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA. 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 1988-11-29 under 510(k) number K884168. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA.?

ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA. is a medical device that received FDA 510(k) clearance on 1988-11-29. The listed applicant is The DU Pont Co.. The 510(k) number is K884168.

When did ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA. receive FDA 510(k) clearance?

ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA. received FDA 510(k) clearance on 1988-11-29, under 510(k) number K884168.

Who is the listed applicant for ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA.?

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 ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA.?

The FDA product code for ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA. is JIS.

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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: JIS)

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.

K122126DIRECT LDL/HDL CHOLESTEROL CALIBRATORRandox Laboratories LimitedK061251DIMENSION VISTA TOTAL IRON BINDING CAPACITY CALIBRATORDade Behring, Inc.K060266DIMENSION IRON CALIBRATORDade Behring, Inc.K053104DIMENSION CARDIOPHASE HIGH SENSITIVITY C-REACTIVE PROTEIN CALIBRATORDade Behring, Inc.K032697DIMENSION TOTAL TRIIODOTHYRONINE CALIBRATOR (RC414)Dade Behring, Inc.K032608GONOTEC CALIBRATION SOLUTION 300 MOSMOL/KG FOR OSMOMETERGonotec Gesellschaft Fuer Mess-Und Regeltechnik MB

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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