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SURGICAL LIGHTSTIC, MODELS, 180 L, AND 180 C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993834
510(k) Type
Traditional
Applicant
CARDIOFOCUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2000
Days to Decision
84 days
Submission Type
Summary

SURGICAL LIGHTSTIC, MODELS, 180 L, AND 180 C

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993834
510(k) Type
Traditional
Applicant
CARDIOFOCUS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2000
Days to Decision
84 days
Submission Type
Summary