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CARDIMAX FX-406U

Page Type
Cleared 510(K)
510(k) Number
K854505
510(k) Type
Traditional
Applicant
BRENTWOOD INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1986
Days to Decision
84 days

CARDIMAX FX-406U

Page Type
Cleared 510(K)
510(k) Number
K854505
510(k) Type
Traditional
Applicant
BRENTWOOD INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1986
Days to Decision
84 days