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SIMULATOR, 10 LEAD ECG

Page Type
Cleared 510(K)
510(k) Number
K761023
510(k) Type
Traditional
Applicant
BIRTCHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1977
Days to Decision
81 days

SIMULATOR, 10 LEAD ECG

Page Type
Cleared 510(K)
510(k) Number
K761023
510(k) Type
Traditional
Applicant
BIRTCHER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1977
Days to Decision
81 days