Last synced on 14 November 2025 at 11:06 pm

SERATEST RF (HEMAGGLUTINATION) KIT

Page Type
Cleared 510(K)
510(k) Number
K855221
510(k) Type
Traditional
Applicant
HEMAGEN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1986
Days to Decision
113 days

SERATEST RF (HEMAGGLUTINATION) KIT

Page Type
Cleared 510(K)
510(k) Number
K855221
510(k) Type
Traditional
Applicant
HEMAGEN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1986
Days to Decision
113 days