Last synced on 30 May 2025 at 11:05 pm

SYNERMED ALKALINE PHOSPHATASE REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904030
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/27/1990
Days to Decision
27 days

SYNERMED ALKALINE PHOSPHATASE REAGENT KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904030
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/27/1990
Days to Decision
27 days