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MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY

Page Type
Cleared 510(K)
510(k) Number
K885188
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/1989
Days to Decision
61 days

MODIFIED RT. ARTRIAL AND 13.5X11.5F CATH. TRAY

Page Type
Cleared 510(K)
510(k) Number
K885188
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/1989
Days to Decision
61 days