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SYNERMED CREATINE KINASE REAGENT KIT

Page Type
Cleared 510(K)
510(k) Number
K930932
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/11/1993
Days to Decision
77 days
Submission Type
Statement

SYNERMED CREATINE KINASE REAGENT KIT

Page Type
Cleared 510(K)
510(k) Number
K930932
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/11/1993
Days to Decision
77 days
Submission Type
Statement