Last synced on 25 January 2026 at 3:41 am

BERICHROM HEPARIN LMW CALIBRATOR, BERICHROM HEPARIN LMW CONTROL 1, AND BERICHROM HEPARIN LMW CONTROL 2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083159
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2009
Days to Decision
91 days
Submission Type
Summary

BERICHROM HEPARIN LMW CALIBRATOR, BERICHROM HEPARIN LMW CONTROL 1, AND BERICHROM HEPARIN LMW CONTROL 2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083159
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2009
Days to Decision
91 days
Submission Type
Summary