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510(k) K994166

GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE ELECTRODE by Gyrus Medical , Ltd. — Product Code KNS

K994166 is an FDA 510(k) premarket notification submitted by Gyrus Medical , Ltd. for the device "GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE ELECTRODE". The FDA issued a decision of Substantially Equivalent on December 27, 1999. The device falls under product code KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories)), a Class II device regulated under 21 CFR 876.4300. Gyrus Medical , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 27, 1999
Date Received
December 9, 1999
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Device Class
Class II
Regulation Number
876.4300
Review Panel
GU
Submission Type

Other clearances by Gyrus Medical , Ltd.

  • K050550 — GYRUS GENERAL PURPOSE ELECTROSURGICAL GENERATOR (November 9, 2005)
  • K050460 — GYRUS PLASMACISION AND PLASMABLEND ELECTRODES (October 25, 2005)
  • K041999 — GYRUS PLASMA SKIN RESURFACING SYSTEM (March 2, 2005)
  • K041633 — GYRUS PLASMACISION LAPAROSCOPIC SPATULA (October 22, 2004)
  • K041285 — GYRUS G3 SYSTEM (GENERATOR, ASSESSORIES, SOMNOPLASTY ELECTRODES AND PLASMACISION (September 10, 2004)
  • K024286 — GYRUS OPEN FORCEPS (November 17, 2003)
  • K031085 — GYRUS PLASMAKINETIC SUPERPULSE SYSTEM (GENERATOR, ACCESSORIES) (July 21, 2003)
  • K031079 — EVEREST BIPOLAR NEEDLE ELECTRODE & GYRUS BIPOLAR NEEDLE ELECTRODE (May 21, 2003)
  • K031082 — EVEREST BIPOLAR L HOOK & PK BIPOLAR L HOOK (May 21, 2003)
  • K031081 — EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS (May 21, 2003)

Other clearances for product code KNS

  • K260962 — Sphincterotome (May 21, 2026)
  • K252388 — Vanquish Water Vapor Ablation Device (November 26, 2025)
  • K252889 — Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M) (November 25, 2025)
  • K250945 — Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Si (October 17, 2025)
  • K250351 — Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical (October 10, 2025)
  • K251104 — SureTome™ SW Sphincterotome with DomeTip (September 29, 2025)
  • K251226 — Aqua Medical RF Vapor Ablation System (August 8, 2025)
  • K250584 — Rezum System (June 11, 2025)
  • K242774 — SpydrBlade Flex Instrument (PRD-RG1-001) (June 6, 2025)
  • K241855 — SB Knife Jr2 (MD-47702 and MD-47702L) (March 26, 2025)

FDA data resources