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15 devices found
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Manufacturer: Talley Group, Ltd.
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Device · Manufacturer · Authorizations
Verified
Status
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Registry
Class
Quattro Plus
Talley Group Ltd.
·
,
United Kingdom
Class IIa
CE/MDD
Active
CE MDD
EUDAMED
IIa
Avance 7703006-00
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Avance 7702003-00
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Avance 7703013-00
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Avance 7703000-00
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Avance 7703014-00
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Avance 7702006-00
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Avance 7702000-00
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Avance 7702013-00
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Talley SD.500 Skin Pressure Evaluator
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class I
FDA 510(k)
K914780
Active
Cleared 19 Dec 1991
Active
510(k)
510(k)
I
Talley Micro System/Talley Ripplebed
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
FDA 510(k)
K914775
Active
Cleared 10 Apr 1992
Active
510(k)
510(k)
II
Oxford Pressure Monitor/Talley Pressure Monitor
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class I
FDA 510(k)
K914776
Active
Cleared 19 Dec 1991
Active
510(k)
510(k)
I
Venturi Gauze Wound Care Sets with Portal Drain
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
FDA 510(k)
K151263
Active
Cleared 19 Feb 2016
Active
510(k)
510(k)
II
Multipulse Sequential Compression Unit
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
FDA 510(k)
K914774
Active
Cleared 11 Feb 1992
Active
510(k)
510(k)
II
VENTURI MiNO TG600/14
Talley Group, Ltd.
·
,
FDA registration: United Kingdom
Class II
FDA 510(k)
K143004
Active
Cleared 5 Jan 2016
Active
510(k)
510(k)
II
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