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ARGYLE DUAL LUMEN UMBILICAL VESSEL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941814
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1994
Days to Decision
171 days
Submission Type
Summary

ARGYLE DUAL LUMEN UMBILICAL VESSEL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941814
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1994
Days to Decision
171 days
Submission Type
Summary