510(k) K241874

Aspiration Catheter (2189) by Hobbs Medical, Inc. — Product Code OCX

K241874 is an FDA 510(k) premarket notification submitted by Hobbs Medical, Inc. for the device "Aspiration Catheter (2189)". The FDA issued a decision of Substantially Equivalent on September 24, 2024. The device falls under product code OCX (Endoscopic Irrigation/Suction System), a Class II device regulated under 21 CFR 876.1500. Hobbs Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 24, 2024
Date Received
June 28, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscopic Irrigation/Suction System
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

To supply sterile water, other solutions and/or suction to endoscopes during endoscopic procedures.