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AMICON DIAFILTER 40. HEMOFILTER

Page Type
Cleared 510(K)
510(k) Number
K840449
510(k) Type
Traditional
Applicant
MEDICAL DEVICE CONSULTANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1984
Days to Decision
51 days

AMICON DIAFILTER 40. HEMOFILTER

Page Type
Cleared 510(K)
510(k) Number
K840449
510(k) Type
Traditional
Applicant
MEDICAL DEVICE CONSULTANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1984
Days to Decision
51 days