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AMP ALKALINE PHOSPHATASE REAGENT KIT

Page Type
Cleared 510(K)
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)
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