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
K010420Substantially Equivalent

Rusch Mmg/o'neil Catheter

Rusch, Inc., Duluth GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K010420 is the FDA 510(k) clearance record for RUSCH MMG/O'NEIL CATHETER, a class II device, cleared for Rusch, Inc. on under FDA product code FCM (Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)). FDA records list 6 510(k) clearances for Rusch, Inc., from to . As of , FDA records show 3 recalls naming K010420.

Clearance record

Decision date
Received
(86 days to decision)
Product code
FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)
Regulation
21 CFR 876.5130
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Rusch, Inc. 2450 Meadowbrook Pkwy., Duluth GA
510(k) summary
Summary
Third party review
No

Clearances, product code FCM

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