Last synced on 14 November 2025 at 11:06 pm

GLUCOSE ANALYZER W/ CHOLESTEROL REAG KIT

Page Type
Cleared 510(K)
510(k) Number
K761089
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1977
Days to Decision
64 days

GLUCOSE ANALYZER W/ CHOLESTEROL REAG KIT

Page Type
Cleared 510(K)
510(k) Number
K761089
510(k) Type
Traditional
Applicant
BECKMAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1977
Days to Decision
64 days