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VYGON DOUBLE LUMEN ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K960795
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1996
Days to Decision
85 days
Submission Type
Statement

VYGON DOUBLE LUMEN ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K960795
510(k) Type
Traditional
Applicant
VYGON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/1996
Days to Decision
85 days
Submission Type
Statement