Last synced on 25 January 2026 at 3:41 am

MEDIFETTE ERGOMETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850870
510(k) Type
Traditional
Applicant
KETRONIC, INC.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
6/12/1985
Days to Decision
103 days

MEDIFETTE ERGOMETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850870
510(k) Type
Traditional
Applicant
KETRONIC, INC.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
6/12/1985
Days to Decision
103 days