Last synced on 30 May 2025 at 11:05 pm

PREDICTA ERYTHROPOIETIN KIT (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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