Aspiration Catheter (2189)— 510(k) K241874

Substantially Equivalent

Hobbs Medical, Inc.

FDA 510(k) clearance K241874 for Aspiration Catheter (2189), Substantially Equivalent on 2024-09-24. Applicant: Hobbs Medical, Inc.. Device class: 2.

Clearance details

Applicant: Hobbs Medical, Inc.
Product code: Code OCX
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2024-06-28
Decision date: 2024-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stafford Springs, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OCX

K251986 — AUXILIARY WATER TUBE MAJ-8552025-09-26
K251997 — Single-Use Biopsy Valve (MAJ-1555)2025-09-25
K242586 — ArgoCap (200.52)2025-05-22
K241704 — Endoscopic Water Pump2025-03-20
K242357 — Water Container (MAJ-901); Water Container (MAJ-902)2024-10-07

More clearances from Hobbs Medical, Inc.

K182927 — Pulmonary Cytology Brush2020-02-07
K093079 — TOUCHSOFT COAGULATOR WITH BANANA FITTING, MODEL 4581 AND WITH UNIVERSAL FITTING, MODEL 4581-U2010-08-02
K030765 — HOBBS MISTIFIER SPRAY CATHETER2003-06-09
K933354 — HOBBS MEDICAL CLEANING BRUSH1993-10-28
K922396 — FUJINON FORCEPS -- MODIFICATION1992-12-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.