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SIGMA DIAGNOSTICS CREATININE REAGENT KIT

Page Type
Cleared 510(K)
510(k) Number
K963534
510(k) Type
Traditional
Applicant
SIGMA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1996
Days to Decision
26 days
Submission Type
Summary

SIGMA DIAGNOSTICS CREATININE REAGENT KIT

Page Type
Cleared 510(K)
510(k) Number
K963534
510(k) Type
Traditional
Applicant
SIGMA DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1996
Days to Decision
26 days
Submission Type
Summary