Last synced on 16 May 2025 at 11:05 pm

EX-TEM. FIB-TEM, AND AP-TEM FOR ROTEM DELTA THROMBOELASTOMETRY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101533
510(k) Type
Traditional
Applicant
Tem Innovations GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/10/2011
Days to Decision
433 days
Submission Type
Summary

EX-TEM. FIB-TEM, AND AP-TEM FOR ROTEM DELTA THROMBOELASTOMETRY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101533
510(k) Type
Traditional
Applicant
Tem Innovations GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/10/2011
Days to Decision
433 days
Submission Type
Summary