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NON STERILE PARENTERAL SUPPLY KIT

Page Type
Cleared 510(K)
510(k) Number
K900857
510(k) Type
Traditional
Applicant
INTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
5/22/1990
Days to Decision
88 days

NON STERILE PARENTERAL SUPPLY KIT

Page Type
Cleared 510(K)
510(k) Number
K900857
510(k) Type
Traditional
Applicant
INTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
5/22/1990
Days to Decision
88 days