Crono Go.

• • Terminated Z-0099-2015 FDA Class II ·initiated 18 Oct 2013

  Product has the potential to have a clear debris on the tip of the needle.

510(k) Number

K052219 ↗

FDA Product Code

FRN

Device Class

Class II

Regulation

21 CFR Part 880.5725

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Crono and Crono Model 30

  Class II

  FDA 510(k) K041414 Active Cleared 8 Jul 2004

• Microjet Crono PCA

  Class II

  FDA 510(k) K013822 Active Cleared 8 May 2002

• Crono F

  Class II

  FDA 510(k) K042085 Active Cleared 17 Sep 2004

• Microjet Quark, Model U100 or U40

  Class II

  FDA 510(k) K013807 Active Cleared 12 Dec 2001

• Microjet Crono

  Class II

  FDA 510(k) K013234 Active Cleared 26 Apr 2002

• Crono S-Pid 50

  Class II

  FDA 510(k) K091042 Active Cleared 12 May 2009

See all devices from Cane S.R.L. →