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KIT, INTRAVENOUS EXTENSION TUBING

Page Type
Cleared 510(K)
510(k) Number
K893120
510(k) Type
Traditional
Applicant
ISLAND MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1989
Days to Decision
93 days

KIT, INTRAVENOUS EXTENSION TUBING

Page Type
Cleared 510(K)
510(k) Number
K893120
510(k) Type
Traditional
Applicant
ISLAND MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1989
Days to Decision
93 days