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DUOPROSS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K052445
510(k) Type
Traditional
Applicant
DUOPROSS MEDITECH CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2005
Days to Decision
89 days
Submission Type
Summary

DUOPROSS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K052445
510(k) Type
Traditional
Applicant
DUOPROSS MEDITECH CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2005
Days to Decision
89 days
Submission Type
Summary