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GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992244
510(k) Type
Traditional
Applicant
Greiner Meditech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1999
Days to Decision
24 days
Submission Type
Summary

GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992244
510(k) Type
Traditional
Applicant
Greiner Meditech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1999
Days to Decision
24 days
Submission Type
Summary