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26 devices found
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Manufacturer: Katecho LLC
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Pediatric Defib K-Pads
Katecho LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K935083
Active
Cleared 25 Jul 1994
Active
510(k)
510(k)
II
K-Disperse
Katecho LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K921679
Active
Cleared 6 Oct 1992
Active
510(k)
510(k)
II
K-Defib/Pace Adult Electrode, Model Kdp-80
Katecho LLC
·
,
FDA registration: United States
Class III
FDA 510(k)
K993745
Active
Cleared 3 Feb 2000
Active
510(k)
510(k)
III
K-Klip
Katecho LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K940801
Active
Cleared 3 Aug 1994
Active
510(k)
510(k)
II
K-Defib/Pace Adult Electrode, Model Kdp-85
Katecho LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K012404
Active
Cleared 12 Oct 2001
Active
510(k)
510(k)
II
Defib K-Pads
Katecho LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K895662
Active
Cleared 18 Jan 1990
Active
510(k)
510(k)
II
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Showing 21-26 of 26