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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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