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WELL LEAD REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K073383
510(k) Type
Traditional
Applicant
WELL LEAD MEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2008
Days to Decision
220 days
Submission Type
Summary

WELL LEAD REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K073383
510(k) Type
Traditional
Applicant
WELL LEAD MEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2008
Days to Decision
220 days
Submission Type
Summary