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COAGUCHEK PRO SYSTEM, APTT TEST CARTRIDGES FOR COAGUCHEK PRO SYSTEM, APTT CONTROLS FOR COAGUCHEK PRO SYSTEM, COAGUCHEK P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983892
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS/BOEHRINGER MANNHEIM GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1999
Days to Decision
161 days
Submission Type
Summary

COAGUCHEK PRO SYSTEM, APTT TEST CARTRIDGES FOR COAGUCHEK PRO SYSTEM, APTT CONTROLS FOR COAGUCHEK PRO SYSTEM, COAGUCHEK P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983892
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS/BOEHRINGER MANNHEIM GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/1999
Days to Decision
161 days
Submission Type
Summary