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ARTERIOVENOUS BLOOD TUBING SET FOR

Page Type
Cleared 510(K)
510(k) Number
K823881
510(k) Type
Traditional
Applicant
AMICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1983
Days to Decision
21 days

ARTERIOVENOUS BLOOD TUBING SET FOR

Page Type
Cleared 510(K)
510(k) Number
K823881
510(k) Type
Traditional
Applicant
AMICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1983
Days to Decision
21 days