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NEOCATH 1000 UMBILICAL ARTERY OXYGEN MONITORING SY

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