510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K030502Substantially Equivalent

14.5F X 55Cm Hemo-Flow Double Lumen Catheter, Models Hfs-55, Hft-55

Medcomp, Harleysville PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030502 is the FDA 510(k) clearance record for 14.5F X 55CM HEMO-FLOW DOUBLE LUMEN CATHETER, MODELS HFS-55, HFT-55, a class II device, cleared for Medcomp on under FDA product code MSD (Catheter, Hemodialysis, Implanted). FDA records list 40 510(k) clearances for Medcomp, from to . As of , FDA records show 2 recalls naming K030502.

Clearance record

Decision date
Received
(90 days to decision)
Product code
MSD Catheter, Hemodialysis, Implanted
Regulation
21 CFR 876.5540
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medcomp 1499 Delp Dr., Harleysville PA
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