ClearanceBrief
Company ยท US

Diagnon Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1986. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CDDRadioassay, Vitamin B122
CGNAcid, Folic, Radioimmunoassay1
GQLAntisera, Fluorescent, Herpesvirus Hominis 1,21
JSNCulture Media, Propagating Transport1
LIODevice, Specimen Collection1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 4, 1986K860967VIRTRAN VIRAL TRANSPORTER (MODIFIED)
Diagnon Corp.
JSN
Oct 10, 1985K851635DIAGNON HERPES IMMUNOPEROXIDASE TYPING TEST
Diagnon Corp.
GQL
Aug 21, 1985K851377DIAGNON MONOCOMBO VITAM. B12[57CO]/FOLATE[125I] RA
Diagnon Corp.
CDD
Jun 21, 1985K851378VIRTRAN VIRAL TRANPORTER
Diagnon Corp.
LIO
Jun 22, 1984K841302DIAGNON FOLATE 125I RIA KIT
Diagnon Corp.
CGN
Dec 8, 1983K832717DIAGNON B12 57CO RIA KIT
Diagnon Corp.
CDD

Latest recalls

DateFirm and productCodeLinked 510(k)
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