Metalaser Vasculase

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K883541 ↗

FDA Product Code

GEX

Device Class

Class II

Regulation

21 CFR Part 878.4810

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Metatech Metal Microclip

  Class II

  FDA 510(k) K881447 Active Cleared 22 Jun 1988

• Metatech Microclip Applicator

  Class I

  FDA 510(k) K882367 Active Cleared 25 Aug 1988

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

  Class II

  FDA 510(k) K903883 Active Cleared 19 Sep 1990

• 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

• Modified Model 2001 Fiber Optics Catheter

  Class II

  FDA 510(k) K883881 Active Cleared 27 Oct 1988

See all devices from Metatech Corp. →