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GLYCOHEMOGLOBIN, IN-VITRO DIAGNOSTIC REAGENT SET

Page Type
Cleared 510(K)
510(k) Number
K860572
510(k) Type
Traditional
Applicant
POINTE SCIENTIFIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/1986
Days to Decision
91 days

GLYCOHEMOGLOBIN, IN-VITRO DIAGNOSTIC REAGENT SET

Page Type
Cleared 510(K)
510(k) Number
K860572
510(k) Type
Traditional
Applicant
POINTE SCIENTIFIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/1986
Days to Decision
91 days