510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K143102Unknown

Multi-Lumen Acute Hemodialysis Catheter for High Volume Infusions

Arrow International, Inc. (Subsidiary of Teleflex, Inc.), Reading PA / Traditional, Unknown
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K143102 is the FDA 510(k) clearance record for Multi-Lumen Acute Hemodialysis Catheter for High Volume Infusions, a class II device, cleared for Arrow International, Inc. (Subsidiary of Teleflex, Inc.) on under FDA product code NIE (Catheter, Hemodialysis, Triple Lumen, Non-Implanted). FDA's definition for product code NIE reads: "Short-term (< 30 days) central venous access for hemodialysis and apheresis, with a third lumen for infusion". FDA records list 10 510(k) clearances for Arrow International, Inc. (Subsidiary of Teleflex, Inc.), from to . As of , FDA records show 2 recalls naming K143102.

Clearance record

Decision date
Received
(268 days to decision)
Product code
NIE Catheter, Hemodialysis, Triple Lumen, Non-Implanted
Regulation
21 CFR 876.5540
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Arrow International, Inc. (Subsidiary of Teleflex, Inc.) 2400 Bernville Rd., Reading PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NIE

Trailing 12 months

FDA records hold no clearances under product code NIE in the trailing twelve months.

FDA records show no clearances under product code NIE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NIE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260