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PREDICTA ERYTHROPOIETIN KIT (MODIFICATION)

Page Type
Cleared 510(K)
510(k) Number
K954898
510(k) Type
Traditional
Applicant
Genzyme Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/1996
Days to Decision
138 days
Submission Type
Summary

PREDICTA ERYTHROPOIETIN KIT (MODIFICATION)

Page Type
Cleared 510(K)
510(k) Number
K954898
510(k) Type
Traditional
Applicant
Genzyme Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/1996
Days to Decision
138 days
Submission Type
Summary