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510(k) K231218

Distal Access Catheter by Accumedical Beijing , Ltd. — Product Code QJP

K231218 is an FDA 510(k) premarket notification submitted by Accumedical Beijing , Ltd. for the device "Distal Access Catheter". The FDA issued a decision of Substantially Equivalent on January 19, 2024. The device falls under product code QJP (Catheter, Percutaneous, Neurovasculature), a Class II device regulated under 21 CFR 870.1250.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 19, 2024
Date Received
April 28, 2023
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 for product code QJP

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  • K253359 — Zenith Distal Access Long Sheath (May 22, 2026)
  • K254178 — SAYA 86 Radial Access Guide Catheter (May 11, 2026)
  • K254046 — BosCATH Support Catheter (April 21, 2026)
  • K254223 — Next Generation 088 Catheter (April 16, 2026)
  • K260938 — PATH BGC (April 15, 2026)
  • K253975 — Radical 6F Access Catheter (April 9, 2026)
  • K253032 — AXS Lift Intracranial Base Catheter (February 11, 2026)
  • K252297 — Toro 88 Superbore Catheter (January 16, 2026)
  • K251097 — V-DAC Catheter (January 6, 2026)

FDA data resources