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GILUCOCHEK REFLECTANCE METER

Page Type
Cleared 510(K)
510(k) Number
K810665
510(k) Type
Traditional
Applicant
LIFESCAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1981
Days to Decision
37 days

GILUCOCHEK REFLECTANCE METER

Page Type
Cleared 510(K)
510(k) Number
K810665
510(k) Type
Traditional
Applicant
LIFESCAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1981
Days to Decision
37 days