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510(k) K991105

ECG ELECTRODE (VARIOUS) by Conmedcorp — Product Code DRX

K991105 is an FDA 510(k) premarket notification submitted by Conmedcorp for the device "ECG ELECTRODE (VARIOUS)". The FDA issued a decision of Substantially Equivalent on November 26, 1999. The device falls under product code DRX (Electrode, Electrocardiograph), a Class II device regulated under 21 CFR 870.2360. Conmedcorp has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 26, 1999
Date Received
April 1, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Electrocardiograph
Device Class
Class II
Regulation Number
870.2360
Review Panel
CV
Submission Type

Other clearances by Conmedcorp

  • K101534 — CONMED ALTRUS THERMAL TISSUE FUSION SYSTEM (November 24, 2010)
  • K061021 — ENTAKE STANDARD AND SAFETY PEG SYSTEM (April 28, 2006)
  • K050992 — CONMED IRRIGATION NOZZLE (July 14, 2005)
  • K050777 — PROFORMA HF 4.5 CANNULA, MODEL 050906, 050907 (April 22, 2005)
  • K050304 — FX WIRE ADVANCED MEASUREMENT GUIDEWIRE (March 8, 2005)
  • K041953 — VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART (August 9, 2004)
  • K021079 — ABCSNARE ELECTROSURGICAL PROBE FOR FLEXIBLE ENDOSCOPES, MODEL 1336XX (July 1, 2002)
  • K021299 — CONMED HEATWAVE HAND-CONTROLLED ELETRODE (June 26, 2002)
  • K020186 — CONMED SYSTEM 5000 ESU (April 12, 2002)
  • K020135 — CONMED SYSTEM 2000 ELECTROSURGICAL GENERATOR, REF: 60-8002; CONMED ESU CART, REF (April 12, 2002)

Other clearances for product code DRX

  • K171244 — Physiotrace (August 23, 2017)
  • K140096 — HMICRO WIRED C-PATCH ELECTRODE, TRADE NAME SUBJECT TO CHANGE (July 24, 2014)
  • K123658 — BIOMODULE 3-M1 (April 24, 2013)
  • K101576 — CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODES (July 22, 2010)
  • K101685 — IP-SET (July 1, 2010)
  • K100129 — AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO X (June 11, 2010)
  • K093327 — INTCO TAB ELECTRODE (May 10, 2010)
  • K100315 — 12 LEAD GLOVE (April 23, 2010)
  • K092744 — NEONATAL ECG ELECTRODE, M203KEN (December 10, 2009)
  • K092389 — DISPOSAL ECG ELECTRODES, MODEL EASYRODE (October 13, 2009)

FDA data resources