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ACTICLOT C KIT

Page Type
Cleared 510(K)
510(k) Number
K884941
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1989
Days to Decision
105 days

ACTICLOT C KIT

Page Type
Cleared 510(K)
510(k) Number
K884941
510(k) Type
Traditional
Applicant
AMERICAN DIAGNOSTIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1989
Days to Decision
105 days