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FDA 510(k)

THYROXINE CALIBRATOR KIT

K-Number: K921903 · 1992-05-26

ApplicantTudor Laboratories, Inc.
Decision Date1992-05-26
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

THYROXINE CALIBRATOR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Tudor Laboratories, Inc.. It received FDA 510(k) clearance on 1992-05-26 under 510(k) number K921903. 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 THYROXINE CALIBRATOR KIT?

THYROXINE CALIBRATOR KIT is a medical device that received FDA 510(k) clearance on 1992-05-26. The listed applicant is Tudor Laboratories, Inc.. The 510(k) number is K921903.

When did THYROXINE CALIBRATOR KIT receive FDA 510(k) clearance?

THYROXINE CALIBRATOR KIT received FDA 510(k) clearance on 1992-05-26, under 510(k) number K921903.

Who is the listed applicant for THYROXINE CALIBRATOR KIT?

The FDA 510(k) record lists Tudor Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THYROXINE CALIBRATOR KIT?

The FDA product code for THYROXINE CALIBRATOR KIT is JIS.

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Other records listing Tudor Laboratories, Inc. 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.

K921904THYROXINE (FPIA) KITK913240DIGITOXIN (FPIA) KITK895572N-ACETYLPROCAINAMIDE (NAPA) CALIBRATOR KITK895571N-ACETYLPROCAINAMIDE (NAPA) (FPIA) KITK895567PRIMIDONE (FPIA) KITK895569VALPROIC ACID (FPIA) KIT

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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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