Last synced on 30 May 2025 at 11:05 pm

THEREX LOW-PROFILE PORT DETACHED CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933316
510(k) Type
Traditional
Applicant
THEREX CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/23/1994
Days to Decision
231 days
Submission Type
Statement

THEREX LOW-PROFILE PORT DETACHED CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933316
510(k) Type
Traditional
Applicant
THEREX CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/23/1994
Days to Decision
231 days
Submission Type
Statement