Home / 510(k) Clearances / K113757

510(k) K113757

ASPIRE MAX ASPIRATION CATHETER by Control Medical Technology, LLC — Product Code QEZ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 22, 2012
Date Received
December 21, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Aspiration Thrombectomy Catheter
Device Class
Class II
Regulation Number
870.5150
Review Panel
CV
Submission Type

To remove thrombus from the peripheral and/or coronary vasculature through aspiration.

Other clearances by Control Medical Technology, LLC

  • K200629 — Aspire Mechanical Aspirator G (May 29, 2020)
  • K200871 — Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirato (May 4, 2020)
  • K131998 — ASPIRE RX-LP6 ASPIRATION CATHETER (November 26, 2013)

Other clearances for product code QEZ

  • K253925 — Aventus Thrombectomy System (January 15, 2026)
  • K252509 — AlphaVac Multipurpose Mechanical Aspiration System F1885 (November 24, 2025)
  • K251312 — Vesalio Peripheral System (October 24, 2025)
  • K251488 — FLOWRUNNER Aspiration System (July 14, 2025)
  • K243549 — JETi Hydrodynamic Thrombectomy System (April 4, 2025)
  • K250013 — VentiV 7Fr -12Fr MP Mechanical Thrombectomy System (VS7-MP60S, VS7-MP90S, VS8-MP (March 24, 2025)
  • K240397 — AlphaVac MMA F1885 System (H787253020) (April 1, 2024)
  • K232458 — JETi™Hydrodynamic Thrombectomy System (December 19, 2023)
  • K213388 — AlphaVac Multipurpose Mechanical Aspiration (MMA) F1885 System (April 4, 2022)
  • K213565 — JETi AIO Peripheral Thrombectomy System (February 1, 2022)