510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K101843Unknown

Duramax Chronic Hemodialysis Catheter and Procedure Kit

Boston Scientific Corporation, Latham NY / Traditional, Unknown
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K101843 is the FDA 510(k) clearance record for DURAMAX CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT, a class II device, cleared for AngioDynamics, Inc. on under FDA product code MSD (Catheter, Hemodialysis, Implanted). FDA records list 1,110 510(k) clearances for Boston Scientific Corporation, from to . As of , FDA records show 30 recalls naming K101843.

Clearance record

Decision date
Received
(111 days to decision)
Product code
MSD Catheter, Hemodialysis, Implanted
Regulation
21 CFR 876.5540
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
AngioDynamics, Inc. 14 Plz. Dr., Latham NY
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