510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K000125Substantially Equivalent

Jet Port Plus Catheter System

Clinical Plastic Products SA, Rancho Santa Margarita CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000125 is the FDA 510(k) clearance record for JET PORT PLUS CATHETER SYSTEM, a class II device, cleared for Clinical Plastic Products SA on under FDA product code LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular). FDA records list one 510(k) clearance for Clinical Plastic Products SA. As of , FDA records show one recall naming K000125.

Clearance record

Decision date
Received
(85 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
Clinical Plastic Products SA 154 Via Lampara, Rancho Santa Margarita CA
510(k) summary
Summary
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