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NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0

Page Type
Cleared 510(K)
510(k) Number
K081515
510(k) Type
Special
Applicant
NEOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2008
Days to Decision
52 days
Submission Type
Summary

NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0

Page Type
Cleared 510(K)
510(k) Number
K081515
510(k) Type
Special
Applicant
NEOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2008
Days to Decision
52 days
Submission Type
Summary