Diagnon Corp.

FDA Regulatory Profile

Diagnon Corp. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 4, 1986.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K860967VIRTRAN VIRAL TRANSPORTER (MODIFIED)April 4, 1986
K851635DIAGNON HERPES IMMUNOPEROXIDASE TYPING TESTOctober 10, 1985
K851377DIAGNON MONOCOMBO VITAM. B12[57CO]/FOLATE[125I] RAAugust 21, 1985
K851378VIRTRAN VIRAL TRANPORTERJune 21, 1985
K841302DIAGNON FOLATE 125I RIA KITJune 22, 1984
K832717DIAGNON B12 57CO RIA KITDecember 8, 1983