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WELL LEAD ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042683
510(k) Type
Traditional
Applicant
WELL LEAD MEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/2005
Days to Decision
142 days
Submission Type
Summary

WELL LEAD ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042683
510(k) Type
Traditional
Applicant
WELL LEAD MEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/2005
Days to Decision
142 days
Submission Type
Summary