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MILLIPORE DUAL RATE INTRAVENOUS CASSETTE

Page Type
Cleared 510(K)
510(k) Number
K811432
510(k) Type
Traditional
Applicant
MILLIPORE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1981
Days to Decision
52 days

MILLIPORE DUAL RATE INTRAVENOUS CASSETTE

Page Type
Cleared 510(K)
510(k) Number
K811432
510(k) Type
Traditional
Applicant
MILLIPORE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1981
Days to Decision
52 days