Last synced on 14 November 2025 at 11:06 pm

BECKMAN DIATRAC HEMOGLOB A1C ELECTRO KIT, MODIFIED

Page Type
Cleared 510(K)
510(k) Number
K925204
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1993
Days to Decision
98 days
Submission Type
Summary

BECKMAN DIATRAC HEMOGLOB A1C ELECTRO KIT, MODIFIED

Page Type
Cleared 510(K)
510(k) Number
K925204
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1993
Days to Decision
98 days
Submission Type
Summary