510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K030209Substantially Equivalent

Mahurkar Oplus Catheter, Model 13.5 Fr

Kendall, Mansfield MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030209 is the FDA 510(k) clearance record for MAHURKAR OPLUS CATHETER, MODEL 13.5 FR, a class II device, cleared for The Kendall Company on under FDA product code MPB (Catheter, Hemodialysis, Non-Implanted). FDA records list 22 510(k) clearances for The Kendall Company, from to . As of , FDA records show 4 recalls naming K030209.

Clearance record

Decision date
Received
(112 days to decision)
Product code
MPB Catheter, Hemodialysis, Non-Implanted
Regulation
21 CFR 876.5540
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
The Kendall Company 15 Hampshire St., Mansfield MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MPB

Trailing 12 months

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

FDA records show no clearances under product code MPB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MPB, 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