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ECG ARRHYTHMIA STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K810104
510(k) Type
Traditional
Applicant
BELMONT INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1981
Days to Decision
13 days

ECG ARRHYTHMIA STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K810104
510(k) Type
Traditional
Applicant
BELMONT INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1981
Days to Decision
13 days