Last synced on 2 May 2025 at 11:05 pm

C TEC SERIES 9000 E.C.G. ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831977
510(k) Type
Traditional
Applicant
SPEYWOOD MEDICAL, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1983
Days to Decision
81 days

C TEC SERIES 9000 E.C.G. ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831977
510(k) Type
Traditional
Applicant
SPEYWOOD MEDICAL, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1983
Days to Decision
81 days