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Medcomp (Dba Medical Components, Inc.)

FDA Regulatory Profile

Medcomp (Dba Medical Components, Inc.) appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 15, 2017.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K171483ArchFlo CT MidlineDecember 15, 2017
K171618Symetrex Long Term Hemodialysis CatheterNovember 16, 2017
K17133320G x 5/8 Pro-Lock CT Safety Infusion SetJuly 18, 2017

FDA data resources