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BECKMAN DIATRAC HEMOGLOBIN A ELECTROPHORESIS KIT

Page Type
Cleared 510(K)
510(k) Number
K905709
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1991
Days to Decision
276 days

BECKMAN DIATRAC HEMOGLOBIN A ELECTROPHORESIS KIT

Page Type
Cleared 510(K)
510(k) Number
K905709
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1991
Days to Decision
276 days