Last synced on 10 January 2025 at 11:05 pm

EKG, SWITCHING BLADE AND PENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781799
510(k) Type
Traditional
Applicant
BIONEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1979
Days to Decision
126 days

EKG, SWITCHING BLADE AND PENS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781799
510(k) Type
Traditional
Applicant
BIONEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1979
Days to Decision
126 days