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NEOMED SINGLE LUMEN UMBILICAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K073596
510(k) Type
Traditional
Applicant
Neomed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2008
Days to Decision
63 days
Submission Type
Summary

NEOMED SINGLE LUMEN UMBILICAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K073596
510(k) Type
Traditional
Applicant
Neomed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2008
Days to Decision
63 days
Submission Type
Summary