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DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K043581
510(k) Type
Special
Applicant
ACMI CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2005
Days to Decision
65 days
Submission Type
Summary

DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K043581
510(k) Type
Special
Applicant
ACMI CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2005
Days to Decision
65 days
Submission Type
Summary