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EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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