510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K203575Unknown

GlidePath Retro Long-Term Hemodialysis Catheter

C.R. Bard Inc, Tempe AZ / Traditional, Unknown
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K203575 is the FDA 510(k) clearance record for GlidePath Retro Long-Term Hemodialysis Catheter, a class II device, cleared for C.R. Bard, Inc. on under FDA product code MSD (Catheter, Hemodialysis, Implanted). FDA records list 646 510(k) clearances for C.R. Bard, Inc., from to . As of , FDA records show no recalls naming K203575.

Clearance record

Decision date
Received
(206 days to decision)
Product code
MSD Catheter, Hemodialysis, Implanted
Regulation
21 CFR 876.5540
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
C.R. Bard, Inc. 1625 W Third St., Tempe AZ
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