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LUNDIA ALPHA 700 HEMODIALYZER

Page Type
Cleared 510(K)
510(k) Number
K931720
510(k) Type
Traditional
Applicant
C.G.H. MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1994
Days to Decision
456 days
Submission Type
Summary

LUNDIA ALPHA 700 HEMODIALYZER

Page Type
Cleared 510(K)
510(k) Number
K931720
510(k) Type
Traditional
Applicant
C.G.H. MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/7/1994
Days to Decision
456 days
Submission Type
Summary