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CARDICARE MODEL MT-301F & MT-301C

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032714
510(k) Type
Traditional
Applicant
Lumiscope Co., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2003
Days to Decision
50 days
Submission Type
Summary

CARDICARE MODEL MT-301F & MT-301C

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032714
510(k) Type
Traditional
Applicant
Lumiscope Co., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2003
Days to Decision
50 days
Submission Type
Summary