510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K041006Substantially Equivalent

Tandem-Cath Hemodialysis Catheter, Model 10 Fr

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

K041006 is the FDA 510(k) clearance record for TANDEM-CATH HEMODIALYSIS CATHETER, MODEL 10 FR, a class II device, cleared for Kendall on under FDA product code MSD (Catheter, Hemodialysis, Implanted). FDA records list 22 510(k) clearances for Kendall, from to . As of , FDA records show no recalls naming K041006.

Clearance record

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

Clearances, product code MSD

Trailing 12 months

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

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