Last synced on 25 January 2026 at 3:41 am

SYNERMED CREATININE REAGENT KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974909
510(k) Type
Traditional
Applicant
Synermed Intl., Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
2/24/1998
Days to Decision
55 days
Submission Type
Statement

SYNERMED CREATININE REAGENT KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974909
510(k) Type
Traditional
Applicant
Synermed Intl., Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
2/24/1998
Days to Decision
55 days
Submission Type
Statement