510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K030636Substantially Equivalent

C-Port

Clinisurg Vascular Products, LLC, Dallas TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030636 is the FDA 510(k) clearance record for C-PORT, a class II device, cleared for Clinisurg Vascular Products, LLC on under FDA product code LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular). FDA records list one 510(k) clearance for Clinisurg Vascular Products, LLC. As of , FDA records show no recalls naming K030636.

Clearance record

Decision date
Received
(97 days to decision)
Product code
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
Regulation
21 CFR 880.5965
Device class
Class II
Review panel
General Hospital
Applicant
Clinisurg Vascular Products, LLC 5454 Amesbury Dr., #2107, Dallas TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LJT

Trailing 12 months
1 clearance under product code LJT in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LJT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260