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12 devices found
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Manufacturer: Wampole Laboratories
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Class
Indirect Fluorescent (Ifa-Ana)
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K760681
Active
Cleared 21 Oct 1976
Active
510(k)
510(k)
II
Rubella Virus Immunological Test System
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K911444
Active
Cleared 30 Aug 1991
Active
510(k)
510(k)
II
Borrelia Burgdorferi Igg/Igm Elisa Test System
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K965131
Active
Cleared 26 Mar 1997
Active
510(k)
510(k)
II
Mono-Plus(Tm)
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K883004
Active
Cleared 4 Aug 1988
Active
510(k)
510(k)
II
Virogen Cmv Antibody Test
Wampole Laboratories
·
,
FDA registration: United States
Class I
FDA 510(k)
K875101
Active
Cleared 1 Mar 1988
Active
510(k)
510(k)
I
Beta-Tec
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K781794
Active
Cleared 29 Dec 1978
Active
510(k)
510(k)
II
Biocept-G
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K760336
Active
Cleared 12 Nov 1976
Active
510(k)
510(k)
II
Rf Controls
Wampole Laboratories
·
,
FDA registration: United States
Class I
FDA 510(k)
K790986
Active
Cleared 28 Jun 1979
Active
510(k)
510(k)
I
One-Step Hcg
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K882896
Active
Cleared 31 Oct 1988
Active
510(k)
510(k)
II
Mat (Tm) Microalbumin Test
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K875161
Active
Cleared 17 Feb 1988
Active
510(k)
510(k)
II
Ucg-Lyphotest
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K791309
Active
Cleared 30 Jul 1979
Active
510(k)
510(k)
II
Borrelia Burgdorferi Igm Elisa Test System
Wampole Laboratories
·
,
FDA registration: United States
Class II
FDA 510(k)
K965129
Active
Cleared 26 Mar 1997
Active
510(k)
510(k)
II
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