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AMP ALKALINE PHOSPHATASE REAGENT KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931986
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/8/1993
Days to Decision
139 days
Submission Type
Statement

AMP ALKALINE PHOSPHATASE REAGENT KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931986
510(k) Type
Traditional
Applicant
SYNERMED, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/8/1993
Days to Decision
139 days
Submission Type
Statement