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THYROXINE CALIBRATOR KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921903
510(k) Type
Traditional
Applicant
TUDOR LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1992
Days to Decision
35 days
Submission Type
Summary

THYROXINE CALIBRATOR KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921903
510(k) Type
Traditional
Applicant
TUDOR LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1992
Days to Decision
35 days
Submission Type
Summary