Last synced on 2 May 2025 at 11:05 pm

DANNIFLEX MODEL 500TM CPM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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