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INFILTRATION KIT

Page Type
Cleared 510(K)
510(k) Number
K100062
510(k) Type
Abbreviated
Applicant
DMG USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2010
Days to Decision
74 days
Submission Type
Summary

INFILTRATION KIT

Page Type
Cleared 510(K)
510(k) Number
K100062
510(k) Type
Abbreviated
Applicant
DMG USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2010
Days to Decision
74 days
Submission Type
Summary