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RECORDER, HOLTER ELECTROCARDIOGRAM

Page Type
Cleared 510(K)
510(k) Number
K781843
510(k) Type
Traditional
Applicant
HOVIK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1978
Days to Decision
2 days

RECORDER, HOLTER ELECTROCARDIOGRAM

Page Type
Cleared 510(K)
510(k) Number
K781843
510(k) Type
Traditional
Applicant
HOVIK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1978
Days to Decision
2 days