510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K050472Substantially Equivalent

Lysus Infusion System

Ekos Corp., Bothell WA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K050472 is the FDA 510(k) clearance record for LYSUS INFUSION SYSTEM, a class II device, cleared for Ekos Corp. on under FDA product code DRA (Catheter, Steerable). FDA records list 25 510(k) clearances for Ekos Corp., from to . As of , FDA records show no recalls naming K050472.

Clearance record

Decision date
Received
(15 days to decision)
Product code
DRA Catheter, Steerable
Regulation
21 CFR 870.1280
Device class
Class II
Review panel
Cardiovascular
Applicant
Ekos Corp. 22030 20th Ave. SE, Bothell WA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DRA

Trailing 12 months
1 clearance under product code DRA in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260