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510(k) K021537

MULTIPURPOSE NEUROPLUS ELECTRODE, MODEL A10005 by Vermont Medical, Inc. — Product Code GXY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 3, 2003
Date Received
May 10, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Cutaneous
Device Class
Class II
Regulation Number
882.1320
Review Panel
NE
Submission Type

Other clearances by Vermont Medical, Inc.

  • K030073 — VERMED A10021 RESTING EKG TAB ELECTRODE (March 28, 2003)
  • K010638 — NEUROPLUS, MODEL A10040, A10041, A10042, A10043 (May 3, 2001)
  • K921498 — VER MED A10011 PNS DUAL ELEMENT ELECTRODE (June 9, 1993)
  • K915831 — THERMAL PROBE COVER (June 8, 1992)
  • K911687 — VER-MED A10020 RESTING EKG ELECTRODE (October 10, 1991)
  • K910139 — VER-MED A10014 RESTING EKG ELECTRODE & A10021 (August 15, 1991)
  • K905489 — VER-MED A10017 UNIVERSAL ELECTRODE (March 21, 1991)
  • K781430 — PREGELLED DISPOSABLE E.K.G. ELECTRODE (October 31, 1978)

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  • K241160 — CAIs Sensor (CAIs-001) (December 13, 2024)
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