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SERIES 602 CKG RECORDER (MODIFIED)

Page Type
Cleared 510(K)
510(k) Number
K801485
510(k) Type
Traditional
Applicant
CARDIOKINETICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1980
Days to Decision
14 days

SERIES 602 CKG RECORDER (MODIFIED)

Page Type
Cleared 510(K)
510(k) Number
K801485
510(k) Type
Traditional
Applicant
CARDIOKINETICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1980
Days to Decision
14 days