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BRADYCARDIA ALARM

Page Type
Cleared 510(K)
510(k) Number
K813174
510(k) Type
Traditional
Applicant
DOUGLAS SCIENTIFIC PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
77 days

BRADYCARDIA ALARM

Page Type
Cleared 510(K)
510(k) Number
K813174
510(k) Type
Traditional
Applicant
DOUGLAS SCIENTIFIC PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
77 days