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510(k) K020568

AKUPORT M-2 by Vibrant Health — Product Code GZO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 30, 2002
Date Received
February 20, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Galvanic Skin Response Measurement
Device Class
Class II
Regulation Number
882.1540
Review Panel
NE
Submission Type

Other clearances by Vibrant Health

  • K020567 — AKUPORT M1 (May 2, 2002)
  • K020565 — EAV COMBI-2 (April 30, 2002)

Other clearances for product code GZO

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  • K152216 — SudoC (September 24, 2015)
  • K141872 — SUDOSCAN (November 21, 2014)
  • K131568 — SUDO PATH (June 28, 2013)
  • K111308 — ZYTO HAND CRADLE (August 30, 2011)
  • K102166 — ELECTRO INTERSTITIAL SCAN (December 10, 2010)
  • K100233 — SUDOSCAN (June 14, 2010)
  • K053004 — MSAS-VANTAGE (January 13, 2006)
  • K032935 — EPI-SCAN, MODEL P 100 (November 20, 2003)
  • K023355 — ASYRA (June 24, 2003)