Home / 510(k) Clearances / K233982

510(k) K233982

CEREGLIDE 92 Catheter System by Cerenovus, Inc. — Product Code QJP

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 9, 2024
Date Received
December 18, 2023
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Percutaneous, Neurovasculature
Device Class
Class II
Regulation Number
870.1250
Review Panel
NE
Submission Type

To provide vascular access to the neurovasculature for interventional or diagnostic procedures

Other clearances by Cerenovus, Inc.

  • K251828 — CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set (August 22, 2025)
  • K241221 — CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovu (October 16, 2024)
  • K241244 — CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter (October 16, 2024)
  • K233988 — Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set (January 17, 2024)
  • K230726 — CEREGLIDE 92 Intermediate Catheter (November 29, 2023)
  • K221934 — CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set (March 9, 2023)
  • K221930 — CEREGLIDE 71 Intermediate Catheter (March 9, 2023)

Other clearances for product code QJP

  • K253032 — AXS Lift Intracranial Base Catheter (February 11, 2026)
  • K252297 — Toro 88 Superbore Catheter (January 16, 2026)
  • K251097 — V-DAC Catheter (January 6, 2026)
  • K251668 — SurfRider 13 Microcatheter (January 5, 2026)
  • K252213 — Bendit17 Microcatheter (December 3, 2025)
  • K251372 — VersaD Delivery Catheter (October 24, 2025)
  • K252569 — Carrier XL Delivery Catheter (October 22, 2025)
  • K250960 — DUO Microcatheter (September 8, 2025)
  • K251560 — FUBUKI XF-R Neurovascular Long Sheath (June 20, 2025)
  • K251240 — Branchor X Balloon Guide Catheter (June 20, 2025)