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DANNIFLEX MODEL 500TM CPM

Page Type
Cleared 510(K)
510(k) Number
K904735
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1991
Days to Decision
105 days

DANNIFLEX MODEL 500TM CPM

Page Type
Cleared 510(K)
510(k) Number
K904735
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1991
Days to Decision
105 days