Last synced on 14 November 2025 at 11:06 pm

THROMBELASTOGRAPH COAGULATION ANALYZER TEG-5000 SERIES

Page Type
Cleared 510(K)
510(k) Number
K002177
510(k) Type
Traditional
Applicant
HAEMOSCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2000
Days to Decision
57 days
Submission Type
Summary

THROMBELASTOGRAPH COAGULATION ANALYZER TEG-5000 SERIES

Page Type
Cleared 510(K)
510(k) Number
K002177
510(k) Type
Traditional
Applicant
HAEMOSCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2000
Days to Decision
57 days
Submission Type
Summary