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510(k) K221930

CEREGLIDE 71 Intermediate Catheter by Cerenovus, Inc. — Product Code QJP

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 9, 2023
Date Received
July 1, 2022
Clearance Type
Traditional
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.

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  • 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)
  • K233982 — CEREGLIDE 92 Catheter System (May 9, 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)

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  • 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)