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NEOCATH 1000 UMBILICAL ARTERY OXYGEN MONITORING SY

Page Type
Cleared 510(K)
510(k) Number
K895149
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1989
Days to Decision
97 days

NEOCATH 1000 UMBILICAL ARTERY OXYGEN MONITORING SY

Page Type
Cleared 510(K)
510(k) Number
K895149
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1989
Days to Decision
97 days