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PACEMAKER, ANTRIO-VENTRICULAR SEQ.

Page Type
Cleared 510(K)
510(k) Number
K770328
510(k) Type
Traditional
Applicant
AMERICAN PACEMAKER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1977
Days to Decision
11 days

PACEMAKER, ANTRIO-VENTRICULAR SEQ.

Page Type
Cleared 510(K)
510(k) Number
K770328
510(k) Type
Traditional
Applicant
AMERICAN PACEMAKER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/1977
Days to Decision
11 days