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ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES

Page Type
Cleared 510(K)
510(k) Number
K853198
510(k) Type
Traditional
Applicant
MEDICAL DEVICE CONSULTANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1985
Days to Decision
66 days

ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES

Page Type
Cleared 510(K)
510(k) Number
K853198
510(k) Type
Traditional
Applicant
MEDICAL DEVICE CONSULTANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1985
Days to Decision
66 days