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HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT

Page Type
Cleared 510(K)
510(k) Number
K890277
510(k) Type
Traditional
Applicant
OSCOR MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1989
Days to Decision
51 days

HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT

Page Type
Cleared 510(K)
510(k) Number
K890277
510(k) Type
Traditional
Applicant
OSCOR MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1989
Days to Decision
51 days