Last synced on 25 January 2026 at 3:41 am

ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980090
510(k) Type
Traditional
Applicant
Luther Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1998
Days to Decision
74 days
Submission Type
Summary

ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980090
510(k) Type
Traditional
Applicant
Luther Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1998
Days to Decision
74 days
Submission Type
Summary