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EUDAMED
FDA 510(k)
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29 devices found
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Manufacturer: Orion Corp.
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Device · Manufacturer · Authorizations
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Class
Cranex Tome Ceph, Or Cranex Tome
Orion Corporation Soredex
·
,
Finland
(FDA 510(k) applicant)
Class II
FDA 510(k)
K974877
Active
Cleared 27 Mar 1998
Active
510(k)
510(k)
II
Resubmitted Modified Rubalex
Orion Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K901637
Active
Cleared 26 Apr 1990
Active
510(k)
510(k)
II
Dentocult-Sm Culture-Paddle
Orion Corp.
·
,
FDA registration: United States
Class I
FDA 510(k)
K872301
Active
Cleared 11 Sep 1987
Active
510(k)
510(k)
I
Rubalex, Modification
Orion Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K912391
Active
Cleared 4 May 1992
Active
510(k)
510(k)
II
Modified Chlamyset Antigen
Orion Corp.
·
,
FDA registration: United States
Class I
FDA 510(k)
K872744
Active
Cleared 22 Sep 1987
Active
510(k)
510(k)
I
Mamex Dc S SL10/MG14
Orion Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K874040
Active
Cleared 23 Nov 1987
Active
510(k)
510(k)
II
Rotalex
Orion Corp.
·
,
FDA registration: United States
Class I
FDA 510(k)
K860529
Active
Cleared 4 Mar 1986
Active
510(k)
510(k)
I
Immunochemical Assay Of C-Reactive Protein
Orion Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K860679
Active
Cleared 4 Aug 1986
Active
510(k)
510(k)
II
Mamex Dc MG11
Orion Corp.
·
,
FDA registration: United States
Class II
FDA 510(k)
K881505
Active
Cleared 10 Jun 1988
Active
510(k)
510(k)
II
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