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Cardiart Electronic Stethoscope Model DS101 Omni-Steth Electronic Stethoscope Model Omni-Steth

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182196
510(k) Type
Traditional
Applicant
Imediplus, Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
9/11/2018
Days to Decision
28 days
Submission Type
Summary

Cardiart Electronic Stethoscope Model DS101 Omni-Steth Electronic Stethoscope Model Omni-Steth

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182196
510(k) Type
Traditional
Applicant
Imediplus, Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
9/11/2018
Days to Decision
28 days
Submission Type
Summary