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CARDIOLIGHT

Page Type
Cleared 510(K)
510(k) Number
K982448
510(k) Type
Traditional
Applicant
CAPINTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1999
Days to Decision
331 days
Submission Type
Summary

CARDIOLIGHT

Page Type
Cleared 510(K)
510(k) Number
K982448
510(k) Type
Traditional
Applicant
CAPINTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1999
Days to Decision
331 days
Submission Type
Summary