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SHILEY PLEXUS(TM) ADULT HOLLOW FIBER OXYGENATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894630
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1989
Days to Decision
88 days

SHILEY PLEXUS(TM) ADULT HOLLOW FIBER OXYGENATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894630
510(k) Type
Traditional
Applicant
SHILEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1989
Days to Decision
88 days