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EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K962389
510(k) Type
Traditional
Applicant
UNOMEDICAL SDN BHD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1996
Days to Decision
154 days
Submission Type
Statement

EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K962389
510(k) Type
Traditional
Applicant
UNOMEDICAL SDN BHD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1996
Days to Decision
154 days
Submission Type
Statement