Last synced on 6 December 2024 at 11:05 pm

BIVONA ILLUMINATED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933398
510(k) Type
Traditional
Applicant
BIVONA MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1993
Days to Decision
86 days
Submission Type
Summary

BIVONA ILLUMINATED ENDOTRACHEAL TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933398
510(k) Type
Traditional
Applicant
BIVONA MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1993
Days to Decision
86 days
Submission Type
Summary