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ARGYLE DUAL LUMEN UMBILICAL VESSEL CATHETER

Page Type
Cleared 510(K)
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)
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