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EUDAMED
FDA 510(k)
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31 devices found
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Manufacturer: Syncor Intl. Corp.
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Device · Manufacturer · Authorizations
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Class
T3 Uptake
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K841927
Active
Cleared 25 Jun 1984
Active
510(k)
510(k)
II
T3 Ria
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K833853
Active
Cleared 4 Feb 1984
Active
510(k)
510(k)
II
Tsh Ria
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K833910
Active
Cleared 22 Nov 1983
Active
510(k)
510(k)
II
Lh Ria
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K833854
Active
Cleared 13 Jan 1984
Active
510(k)
510(k)
I
2 variants
See all variants of this device
Fsh Ria
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K842444
Active
Cleared 17 Aug 1984
Active
510(k)
510(k)
I
2 variants
Fsh Ria
K833852
Wire Cutters, Brachytherapy-Table Top & Hand Held
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K850726
Active
Cleared 26 Mar 1985
Active
510(k)
510(k)
II
Curietron
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K840127
Active
Cleared 19 Mar 1984
Active
510(k)
510(k)
II
Hcg Ria
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K833851
Active
Cleared 19 Mar 1984
Active
510(k)
510(k)
II
Cesium 137 Endometrial Source
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K850433
Active
Cleared 21 Aug 1985
Active
510(k)
510(k)
II
Tbg Ria
Syncor Intl. Corp.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K842167
Active
Cleared 9 Jul 1984
Active
510(k)
510(k)
II
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Showing 21-31 of 31