Last synced on 14 November 2025 at 11:06 pm

CARDIOMETER

Page Type
Cleared 510(K)
510(k) Number
K780117
510(k) Type
Traditional
Applicant
MED GENERAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1978
Days to Decision
11 days

CARDIOMETER

Page Type
Cleared 510(K)
510(k) Number
K780117
510(k) Type
Traditional
Applicant
MED GENERAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1978
Days to Decision
11 days