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MODEL 2001, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K905029
510(k) Type
Traditional
Applicant
MEDFUSION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/1990
Days to Decision
54 days

MODEL 2001, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K905029
510(k) Type
Traditional
Applicant
MEDFUSION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/1990
Days to Decision
54 days