Home / 510(k) Clearances / K221951

510(k) K221951

Branchor Balloon Guide Catheter by Asahi Intecc Co., Ltd. — Product Code QJP

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 11, 2022
Date Received
July 5, 2022
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 Asahi Intecc Co., Ltd.

  • K252011 — CHIKAI Nexus petit (February 2, 2026)
  • K251560 — FUBUKI XF-R Neurovascular Long Sheath (June 20, 2025)
  • K251240 — Branchor X Balloon Guide Catheter (June 20, 2025)
  • K243383 — CHIKAI Nexus 014 (April 21, 2025)
  • K243733 — SION blue PLUS (April 2, 2025)
  • K241962 — Crossloop (March 27, 2025)
  • K242597 — CROSSLEAD 0.018inch (March 5, 2025)
  • K241702 — CROSSLEAD 0.014inch (February 6, 2025)
  • K241801 — Tornus ES (December 17, 2024)
  • K241510 — CROSSLEAD Tracker (August 14, 2024)

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)