Home / 510(k) Clearances / K231267

510(k) K231267

ClearTip by Finemedix Co., Ltd. — Product Code FCG

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 30, 2023
Date Received
May 2, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Biopsy Needle
Device Class
Class II
Regulation Number
876.1075
Review Panel
GU
Submission Type

Other clearances by Finemedix Co., Ltd.

  • K250994 — ClearTip FNA and FNB Types (August 21, 2025)
  • K242857 — ClearHemograsper (May 21, 2025)
  • K242134 — ClearCap Distal Attachment (August 20, 2024)
  • K202616 — ClearCap Distal Attachment (February 19, 2021)
  • K200217 — ClearEndoclip (October 5, 2020)
  • K183021 — ClearEndoclip (June 28, 2019)
  • K183289 — ClearGrasp Snare (March 6, 2019)
  • K181690 — Clear-Jet Injection Catheter (December 21, 2018)
  • K180363 — Clear-Tip EUS-FNA (November 1, 2018)

Other clearances for product code FCG

  • K252646 — Single-Use Fine Needle Biopsy (FNB) device (NA-U210H) (October 24, 2025)
  • K250994 — ClearTip FNA and FNB Types (August 21, 2025)
  • K241209 — EchoTip AcuCore™ EUS Biopsy Needle (ECHO-BX-19) (July 29, 2024)
  • K231422 — Precision GI (August 28, 2023)
  • K230909 — EchoTip® AcuCore™ Ultrasound Biopsy Needle (ECHO-BX-3-22) (May 30, 2023)
  • K212423 — EndoDrill® Model X (March 29, 2023)
  • K212822 — Disposable Coaxial Biopsy Needle (July 6, 2022)
  • K212819 — Disposable Biopsy Refill Needle (July 6, 2022)
  • K210476 — EchoTip Ultra Endoscopic Ultrasound Needle, EchoTip ProCore HD Ultrasound Biopsy (May 20, 2021)
  • K191472 — Biopsy Needle (January 29, 2020)