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WIRE REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K932647
510(k) Type
Traditional
Applicant
VITAID, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/1993
Days to Decision
153 days
Submission Type
Statement

WIRE REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K932647
510(k) Type
Traditional
Applicant
VITAID, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/1993
Days to Decision
153 days
Submission Type
Statement