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LARYNGEAL SURFACE ELECTRODE-ENDOTRACHEAL TUBE, M-500-ET, LSE-ET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003745
510(k) Type
Traditional
Applicant
RLN SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2001
Days to Decision
43 days
Submission Type
Summary

LARYNGEAL SURFACE ELECTRODE-ENDOTRACHEAL TUBE, M-500-ET, LSE-ET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003745
510(k) Type
Traditional
Applicant
RLN SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2001
Days to Decision
43 days
Submission Type
Summary