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CREATININE-PO REAGENT KIT

Page Type
Cleared 510(K)
510(k) Number
K943924
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/20/1994
Days to Decision
39 days
Submission Type
Statement

CREATININE-PO REAGENT KIT

Page Type
Cleared 510(K)
510(k) Number
K943924
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/20/1994
Days to Decision
39 days
Submission Type
Statement