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11 devices found
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Manufacturer: Viztek, Inc.
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Class
ViZion DR + Wireless
Viztek, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K152279
Active
Cleared 10 Sep 2015
Active
510(k)
510(k)
II
2 variants
ViZion DR + Wireless
K160810
Onyx-Rad Telemedicine Pacs
Viztek, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K003607
Active
Cleared 15 Feb 2001
Active
510(k)
510(k)
II
Vizion + Dr
Viztek, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K123644
Active
Cleared 11 Jan 2013
Active
510(k)
510(k)
II
Vizion Dr
Viztek, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K112661
Active
Cleared 20 Oct 2011
Active
510(k)
510(k)
II
Opal-Rad
Viztek, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K063337
Active
Cleared 12 Dec 2006
Active
510(k)
510(k)
II
Vizion Ultra
Viztek, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K133139
Active
Cleared 3 Apr 2014
Active
510(k)
510(k)
II
Exa
Viztek, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K142919
Active
Cleared 16 Dec 2014
Active
510(k)
510(k)
II
Viztek Dr, Models: DR1000, DR3000, DR4000
Viztek, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K082604
Active
Cleared 21 Nov 2008
Active
510(k)
510(k)
II
Vizion Dr
Viztek, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K102123
Active
Cleared 24 Jan 2011
Active
510(k)
510(k)
II
Viztek Wl
Viztek, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K091752
Active
Cleared 12 Nov 2009
Active
510(k)
510(k)
II
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