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Dmc Medical, Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K103736
DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE
June 10, 2011
K992932
CIPA (ADULTS) CIPI (INFANTS)
June 7, 2000
K000704
DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)
May 19, 2000