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DANNIFLEX 400I

Page Type
Cleared 510(K)
510(k) Number
K870510
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1987
Days to Decision
21 days

DANNIFLEX 400I

Page Type
Cleared 510(K)
510(k) Number
K870510
510(k) Type
Traditional
Applicant
BUCKMAN CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1987
Days to Decision
21 days