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510(k) K113454

14 WIRE STANDARD, 14 WIRE LS by Micro Therapeutics, Inc. — Product Code DQX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 2012
Date Received
November 21, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Wire, Guide, Catheter
Device Class
Class II
Regulation Number
870.1330
Review Panel
CV
Submission Type

Other clearances by Micro Therapeutics, Inc.

  • K113289 — ORION MICRO CATHETER (August 1, 2012)
  • K090870 — ECHELON MICRO CATHETER, MODELS 105-5092-150SA, 145-5092-150SA AND 190-5092-150SA (May 1, 2009)
  • K090046 — CONCERTO DETACHABLE COIL SYSTEM (February 27, 2009)
  • K081465 — AXIUM DETACHABLE COIL SYSTEM (August 19, 2008)
  • K060747 — FX DETACHABLE COIL SYSTEM (April 24, 2007)
  • K060625 — NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR (April 20, 2006)
  • K051990 — ECHELON MICRO CATHETER (January 4, 2006)
  • K051560 — NEXUS DETACHABLE COIL, MULTI-DIAMETER CSR AND HELIX SUPER SOFT CSR (June 28, 2005)
  • K051425 — NEXUS DETACHABLE COIL SYSTEM, HELIX SUPER SOFT CSR (June 22, 2005)
  • K050543 — NEXUS DETACHABLE COIL SYSTEM (April 27, 2005)

Other clearances for product code DQX

  • K253262 — EmeryGlide™ (EG18008901) (March 6, 2026)
  • K253847 — Splashwire Hydrophilic Guide Wire (MSWSTD35150J3) (January 31, 2026)
  • K251385 — InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire (IQ (January 21, 2026)
  • K252674 — Solo Pace Fusion System (SOLOFUSE1) (January 9, 2026)
  • K251596 — Lunderquist Extra Stiff Wire Guide (November 9, 2025)
  • K250203 — SureAx-Guide™ (October 17, 2025)
  • K250031 — Amplatzer Guidewire (October 3, 2025)
  • K251181 — Splashwire Hydrophilic Guide Wire (MSWSTD35180J1O5); Splashwire Hydrophilic Guid (August 29, 2025)
  • K250552 — Hi-Torque Command 14 ST Guide Wire and Hi-Torque Command 14 MT Guide Wire (July 25, 2025)
  • K250075 — Medtronic Stedi Extra Support Guidewire (June 13, 2025)