Last synced on 14 November 2025 at 11:06 pm

GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE

Page Type
Cleared 510(K)
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)
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