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Dilon Technologies, Inc.

FDA Regulatory Profile

Dilon Technologies, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 3, 2011.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K110384DILON 6800 ACELLA (ACELLA)May 3, 2011
K082588GAMMALOC SYSTEM, MODEL 03-00001December 11, 2009
K984466DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5March 16, 1999

FDA data resources