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TANDEM-E FERRITIN CALIBRATION VERIFICATION CONROL

Page Type
Cleared 510(K)
510(k) Number
K921252
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1992
Days to Decision
123 days
Submission Type
Summary

TANDEM-E FERRITIN CALIBRATION VERIFICATION CONROL

Page Type
Cleared 510(K)
510(k) Number
K921252
510(k) Type
Traditional
Applicant
HYBRITECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1992
Days to Decision
123 days
Submission Type
Summary