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ROTEM DELTA THROMBOELASTOMETRY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K083842
510(k) Type
Traditional
Applicant
PENTAPHARM GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/23/2010
Days to Decision
454 days
Submission Type
Summary

ROTEM DELTA THROMBOELASTOMETRY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K083842
510(k) Type
Traditional
Applicant
PENTAPHARM GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/23/2010
Days to Decision
454 days
Submission Type
Summary