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CONTINUOUS FLUSH DEVICE

Page Type
Cleared 510(K)
510(k) Number
K831730
510(k) Type
Traditional
Applicant
AMERICAN PHARMASEAL DIV. AHSC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1983
Days to Decision
48 days

CONTINUOUS FLUSH DEVICE

Page Type
Cleared 510(K)
510(k) Number
K831730
510(k) Type
Traditional
Applicant
AMERICAN PHARMASEAL DIV. AHSC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1983
Days to Decision
48 days