Event Marker & a Second Pressure Trend Output

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K883518 ↗

FDA Product Code

GWM

Device Class

Class II

Regulation

21 CFR Part 882.1620

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Metatech Metal Microclip

  Class II

  FDA 510(k) K881447 Active Cleared 22 Jun 1988

• Metatech Microclip Applicator

  Class I

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• Metalaser Vasculase

  Class II

  FDA 510(k) K883541 Active Cleared 4 Nov 1988

• Vasculase(R) Copper Vapor Laser Syst, Pigment Les

  Class II

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• Easytem Ear Thermometer, Model Bt-020

  Class II

  FDA 510(k) K020520 Active Cleared 6 Aug 2002

• Easytem Duo, Forehead/Ear Thermometer, Model Bt-021

  Class II

  FDA 510(k) K033077 Active Cleared 30 Apr 2004

See all devices from Metatech Corp. →