Last synced on 4 July 2025 at 11:05 pm

OMNICATH IMPLANTED CATHETER AND DEPOT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911775
510(k) Type
Traditional
Applicant
OMNITRON INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1991
Days to Decision
37 days

OMNICATH IMPLANTED CATHETER AND DEPOT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K911775
510(k) Type
Traditional
Applicant
OMNITRON INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1991
Days to Decision
37 days