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PROLITH MODEL 21S CARDIAC PULSE GEN.

Page Type
Cleared 510(K)
510(k) Number
K770212
510(k) Type
Traditional
Applicant
EDWARDS PACEMAKER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1977
Days to Decision
37 days

PROLITH MODEL 21S CARDIAC PULSE GEN.

Page Type
Cleared 510(K)
510(k) Number
K770212
510(k) Type
Traditional
Applicant
EDWARDS PACEMAKER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1977
Days to Decision
37 days