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SYNERMED CREATINE KINASE REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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